WE CARE SKILLED NURSING FACILITY

21863 VALLEJO STREET, HAYWARD, CA 94541 (510) 750-1245
For profit - Corporation 28 Beds Independent Data: November 2025
Trust Grade
80/100
#265 of 1155 in CA
Last Inspection: February 2025

Within standard 12-15 month inspection cycle. Federal law requires annual inspections.

Overview

We Care Skilled Nursing Facility has a Trust Grade of B+, which means it is considered above average and recommended for care. It ranks #265 out of 1155 facilities in California, placing it in the top half, and #24 out of 69 in Alameda County, indicating it is one of the better options locally. Unfortunately, the facility's trend is worsening, with the number of issues increasing from 1 in 2024 to 11 in 2025, signaling potential concerns about care quality. While staffing is average with a 3/5 star rating and a turnover rate of 44%, there are no fines on record, which is a positive indicator. However, specific incidents, such as unlabeled and undated food storage that risks foodborne illnesses and medication errors that could compromise resident health, highlight areas needing improvement. Overall, the facility has strengths in its overall quality ratings but also faces challenges that families should consider.

Trust Score
B+
80/100
In California
#265/1155
Top 22%
Safety Record
Low Risk
No red flags
Inspections
Getting Worse
1 → 11 violations
Staff Stability
○ Average
44% turnover. Near California's 48% average. Typical for the industry.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most California facilities.
Skilled Nurses
⚠ Watch
Each resident gets only 23 minutes of Registered Nurse (RN) attention daily — below average for California. Fewer RN minutes means fewer trained eyes watching for problems.
Violations
⚠ Watch
27 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★★
5.0
Overall Rating
★★★☆☆
3.0
Staff Levels
★★★★★
5.0
Care Quality
★★★★☆
4.0
Inspection Score
Stable
2024: 1 issues
2025: 11 issues

The Good

  • 5-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (44%)

    4 points below California average of 48%

Facility shows strength in quality measures, fire safety.

The Bad

Staff Turnover: 44%

Near California avg (46%)

Typical for the industry

The Ugly 27 deficiencies on record

Feb 2025 11 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0685 (Tag F0685)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure for one of four sampled residents (Resident 14)...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure for one of four sampled residents (Resident 14), reviewed for communication deficit, received proper treatment to maintain hearing ability when hearing loss was not addressed by ht facility. This failure had the potential to result in the delayed access to hearing services. Findings: During a review of Resident 14's admission Record (AR), the AR indicated Resident was initially admitted to the facility in September 2024 with diagnoses that included muscle weakness, difficulty walking and end stage renal disease (ESRD, the final stage of long-term kidney disease when the kidneys are no longer sufficiently able to remove waste products and excess water to support the body's needs). During a review of Resident 14's Minimum Data Assessment (MDS, an assessment tool used to direct resident care) dated 9/18/24, the MDS indicated Resident 14 had adequate hearing. During a review of another MDS dated [DATE], the MDS indicated Resident 14 had moderate difficulty hearing (speaker has to increase volume and speak distinctly). Resident 14's most recent MDS dated [DATE] also indicated moderate difficulty hearing and a Brief Interview for Mental Status (BIMS, a scoring system to determine the resident's cognitive status in regard to attention, orientation, and ability to register and recall information) score of 14. A score of 13-15 is an indication of intact cognitive status. During an observation and concurrent interview on 2/24/25 at 11:46 a.m. with Resident 14, Resident 14 asked this writer to repeat what was said and to speak louder. Resident 14 stated not being able to hear. During a confidential group interview on 2/25/25 at 10:18 a.m., Resident 14 looked on while appearing confused when another resident spoke. Resident 14 stated not being able to hear what the other resident had said. During an interview and concurrent review of Resident 14's comprehensive care plan on 2/26/25 at 9:35 a.m. with Assistant Director of Nursing (ADON), ADON stated Resident 14 had already been hard of hearing since being admitted from an independent living facility, but the personal inventory effects did not indicate Resident 14 was admitted with hearing aids. ADON stated a comprehensive care plan was not initiated to address inability to hear especially that the MDS already indicated Resident 14 had moderate difficulty hearing. During an interview and concurrent record review on 2/26/25 at 9:44 a.m. with Social Services Director (SSD), SSD stated Resident 14 was admitted to the facility for long term stay. SSD stated Resident 14 was sent to the hospital and returned to the facility with moderate difficulty in hearing. SSD stated having to write on a piece of paper when communicating with Resident 14. SSD stated she did not know whether Resident 14 had a hearing aid while at the independent living facility and had not followed up if Resident 14's insurance could pay for hearing aid. SSD stated Resident 14 was admitted in September 2024 with adequate hearing but after Resident 14 went to the hospital and returned in October 2024, Resident 14 had been hard of hearing. SSD stated having told the DON about the change but could not show documentation that it was discussed with Nursing Department. SSD stated the normal process was for Nursing to flush the resident's ear to make sure there was no foreign objects in the ear, inform the doctor and the resident's responsible party, and set up appointment with audiology doctor. SSD stated none of these was done for Resident 14. During an interview on 2/26/25 at 10:03 a.m. with Certified Nursing Assistant (CNA) 1, CNA 1 stated she had to speak loudly into Resident 14's right ear during care. During an observation and concurrent interview on 2/26/25 at 10:05 a.m. with Resident 14, while in the activity room, Resident 14 stated it was bothersome that she could not have normal conversation where people did not have to be within inches from her face. Resident 14 was staring at the TV but said she could not hear what the lady on the screen said because the volume was not turned up.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Incontinence Care (Tag F0690)

Could have caused harm · This affected 1 resident

Based on interview and record review, the facility failed to provide treatment and services to prevent urinary tract infection for one of one sampled resident (Resident 70), when staff did not follow-...

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Based on interview and record review, the facility failed to provide treatment and services to prevent urinary tract infection for one of one sampled resident (Resident 70), when staff did not follow-up on Resident 70's complaint of painful urination. This failure had the potential to result in delayed treatment. Findings: During a review of Resident 70's admission Record (AR), the AR indicated Resident 70 was admitted to the facility in December 2024 with diagnoses that included chronic kidney disease (a long-term condition where the kidneys gradually lose their ability to filter waste products and excess fluid from the blood), muscle weakness, and diabetes mellitus (a chronic/long-term disease in which the body cannot regulate the amount of sugar in the blood). During review of Resident 70's Minimum Data Set (MDS, an assessment tool used to direct resident care) dated 12/27/24, the MDS indicated a Brief Interview for Mental Status (BIMS, a scoring system to determine the resident's cognitive status in regard to attention, orientation, and ability to register and recall information) score of 12. A score of 8-12 is an indication of moderate impairment whereas 13-15 indicates intact cognitive status. The MDS also indicated Resident 70 was frequently incontinent of urine and was dependent on staff for toileting hygiene (ability to maintain perineal [the area of the body between the anus and the vulva in females, and between the anus and the scrotum in males] hygiene, adjust clothes before and after voiding or having a bowel movement). During an interview on 2/24/25 at 11:31 a.m. with Resident 70, Resident 70 stated how it hurts so much when trying to pass urine. Resident 70 stated the staff knew about it. During an interview on 2/27/25 at 2:03 p.m. with Certified Nursing Assistant (CNA) 2, CNA 2 stated Resident 70's urine smelled strange and she had told Licensed Vocational Nurse (LVN) 2 about it on 2/25/25. CNA 2 also stated Resident 70 complained of painful urination. During an interview and concurrent review of the clinical record on 2/27/25 at 2:22 p.m. with LVN 2, LVN 2 stated, on 2/25/25, she sent a text message to Resident 70's Attending Physician (AP) regarding Resident 70's status. LVN 2 stated, AP ordered urine specimen collection, but Resident 70 refused the procedure. LVN 2 stated AP ordered to continue to encourage Resident 70 to agree with urine collection. LVN 2 stated there was no documentation about Resident 70's change of condition in the clinical record. LVN 2 stated the policy was for the licensed staff to complete an SBAR (Situation, Background, Assessment and Recommendation, a standardized method of communication among healthcare providers to enhance patient safety, improve clarity in critical situations and reduce errors in communication), call the physician, and initiate a care plan, to alert everybody to follow-up. LVN 2 stated she did not complete an SBAR, there was no written physician's order for urine collection and there was no care plan in the clinical record. LVN 2 stated, at the time of the interview, no follow-up had been done. During a joint interview and concurrent record review on 2/27/25 at 2:27 p.m. with Director of Nursing (DON) and Assistant Director of Nursing (ADON), both stated, for any new concern regarding a resident, an SBAR should be completed and any order related to the concern should be entered into the system so that the following shift would be able to monitor, follow-up, and in this case, continue to encourage Resident 70's compliance. During a review of the facility's policy and procedure (P&P) titled S-BAR Communication, undated, the P&P indicated the facility will use SBAR technique for all critical communications, including shift hand-offs, patient status updates, and emergency situations to ensure clear and structured communications. An SBAR is used for nurse-to-physician communication regarding a patient's change in condition, and shift to shift hand-offs.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

Based on observation, interview and record review, the facility failed to monitor and assist in maintaining a sufficient food and fluid intake and for one of 20 sampled residents (Resident 9), when Re...

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Based on observation, interview and record review, the facility failed to monitor and assist in maintaining a sufficient food and fluid intake and for one of 20 sampled residents (Resident 9), when Resident 9 was not offered sufficient fluid intake and weight loss was not addressed to maintain proper hydration and health. This failure had the potential to result dehydration (dangerous loss of body fluid causes by illness or inadequate fluid intake) and further decline in Resident 9's health condition. Findings: During a review of Resident 9's admission Record', printed on 2/27/25, the admission Record indicated Resident 9 was admitted to the facility in February 2025 with multiple diagnoses including urinary tract infection (an infection of the urinary tract, which includes the kidneys, ureters, bladder, and urethra) and Parkinson's disease (a brain disorder that causes unintended or uncontrollable movements, such as shaking, stiffness, and difficulty with balance and coordination. Symptoms usually begin gradually and worsen over time. As the disease progresses, people may have difficulty walking and talking. They may also have mental and behavioral changes, sleep problems, depression, memory difficulties, and fatigue.) During a review of Resident 9's Brief Interview for Mental Status (BIMS, is a scoring system used to determine the resident's cognitive status regarding attention, orientation, and ability to register and recall information. A BIMS score zero to seven is an indication of severe cognitive impact.), dated 2/7/25, the record indicated Resident 9's BIMS score was 2. During a review of Resident 9's Minimum Data Set (MDS, a resident assessment instrument used to identify resident care problems to be addressed in an individualized care plan.) dated 2/7/25, the MDS assessment section GG (Functional Abilities and Goal) indicated Resident 9 needed substantial or maximal assistance (helper does more than half the effort) to maintain eating and drinking. During a review of Resident 9's Care Plan, dated 2/3/25, the care plan indicated Resident 9 was at risk for dehydration or electrolyte imbalance related to dementia (a loss of brain function that occurs with certain diseases, affecting one or more brain functions such as memory, thinking, language, judgment, or behavior). During a review of Resident 9's record of fluid intake, dated 2/13/25 to 2/25/25, the record indicated the following amount of fluid that was consumed by Resident 9: 2/13/25 230 milliliters (ml) 2/20/25 300ml 2/14/25 560ml 2/21/25 340ml 2/15/25 600ml 2/22/25 840ml 2/16/25 600ml 2/23/25 840ml 2/17/25 600ml 2/24/25 840ml 2/18/25 700ml 2/25/25 960ml 2/19/25 720ml During a record review of the Registered Dietician's (RD) Progress Notes, dated 2/18/25, the Progress Notes indicated that Resident 9 had a notable weight loss of 2.4lbs (pounds) in one week was likely due to very low food and fluid intake. The RD's progress notes indicated Resident 9 was only consuming 0-25% of her meals and it was not enough to meet Resident 9's needs. The progess notes also indicated that RD had a recommendation for Resident 9 to maintain fluid intake between 1240ml-1485ml a day. During an observation and interview on 2/24/25 at 12:34 p.m. with Resident 9, Resident 9 was being fed by Resident 9's daughter and responsible party (RP) during lunch time. RP stated Resident 9 had an order for pureed diet (foods have a soft, pudding-like consistency) and regular liquid. RP stated Resident 9 needed assistance in feeding because of her dementia. During an interview on 2/26/25 at 9:37 a.m. with Certified Nurse Assistant (CNA) 1, CNA 1 stated Resident 9 needed someone to directly supervise and feed Resident 9 during mealtimes. CNA 1 stated Resident 9 had to be offered fluids otherwise, Resident 9 would not have had anything to drink. CNA 1 stated Resident 1 could have had symptoms of dehydration including confusion, blurry vision, dry skin and urinary tract infection (UTI, a bacterial infection in any part of the urinary system). During an interview on 2/26/25 at 11:12 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 stated Resident 9 had history of low meal and fluid intake. LVN 2 stated Resident 9 needed encouragement to eat and drink. LVN 2 stated she did not know if Resident 9 was meeting enough fluid intake because she was not aware on how much hydration Resident 9 should have been receiving in a day. LVN 2 further stated there was also no order from the physician to provide a supplement or nutritional drink to Resident 9. LVN 2 stated without proper hydration and nutrition, Resident could have been fatigued and Resident 9 would have not been able to participate in her physical therapy. During a concurrent record review and interview on 2/26/25 at 12:54 p.m. with the Director of Nursing (DON), the Registered Dietician's (RD) Progress Notes, dated 2/18/24, and Resident 9's record of fluid intake, dated from 2/13/25 to 2/25/25, were reviewed. The DON stated when Resident 9 was admitted to the facility, they were already aware that Resident 9 had very low food and fluid intake because Resident 9 had altered level of consciousness on the week Resident 9 was admitted . The DON stated Resident 9 was treated with intravenous (IV, through the vein) therapy for dehydration. The DON stated she was not aware that Resident 9 had weight loss of 2.4lbs in one week and that RD had a recommendation to maintain Resident's 9 fluid intake between 1240ml-1485ml a day. The DON stated she did not read the RD's progress notes. The DON stated Resident 9's fluid intake recorded by the CNAs were also not meeting and maintaining Resident 9's hydration . The DON stated Resident 9's hydration and nutrition intake should have been maintained and monitored consistently because Resident 9's condition could have gotten worse. During an interview on 2/28/25 at 10:31 a.m. with the ADON, the ADON stated Resident 9's weights should have been monitored upon admission and every week. The ADON further stated she discontinued the order for Resident 9's weekly weights monitoring by mistake. The ADON stated Resident 9 was last weighed on 2/18/25 that had a weight loss of 2.4 lbs. The ADON stated when a weight loss was identified, the IDT should have created a plan to resolve Resident 9's weight loss. The ADON stated they also did not develop a care plan for Resident 9's weight loss even though they knew Resident 9 was high risk for malnutrition due to very low food and fluid intake. The ADON stated Resident 9 had the risk to have complications such as dehydration and electrolyte imbalances (occurs when the body's minerals were too low or hight that may cause fatigue, headache, dizziness, etc.) because hydration and weight loss were not monitored. During a record review of the facility's policy and procedure (P&P), titled, Resident Hydration and Prevention of Dehydration, dated October 2017, the P&P indicated, This facility will provide adequate hydration and to prevent and treat dehydration .Nurses' aides will provide and encourage intake of bedside snack, meals, and fluids on a daily and routine basis as part daily care .Aides will report intake of less than 1200ml/day to nursing staff . During a record review of the facility's P&P, titled, Weight Assessment and Intervention, dated March 2022, the P&P indicated, Resident weights are monitored for undesirable or unintended weight loss or gain .The physician and the multidisciplinary team identify conditions and medications that maybe causing weight loss or increasing the risk of weight loss .a. cognitive or functional decline .b. chewing or swallowing abnormalities .h. fluid and nutrient loss .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0694 (Tag F0694)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure that one of one sampled resident (Resident 1) with peripherally inserted central catheter (PICC, a long, thin, flexibl...

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Based on observation, interview, and record review, the facility failed to ensure that one of one sampled resident (Resident 1) with peripherally inserted central catheter (PICC, a long, thin, flexible tube that is placed into a small vein in the upper arm and moved forward until it is in a larger vein near the heart) received appropriate care and services consistent with professional standards of practice and in accordance with physician orders when Resident 1's PICC line dressing was not changed and monitored for complications. These failures had the potential for Resident 1 to develop complications such as infection and dislodgement (PICC line catheter displacement). Findings: During a record review of Resident 1's admission Record', printed on 2/27/25, the admission Record indicated Resident 1 was admitted to the facility in December 2024 with diagnosis of cellulitis (bacterial skin infection) of right and left lower limbs. During a record review of Resident 1's Order Summary, dated 2/27/25, the order summary indicated Resident 1 had an order to change the PICC line dressing every 7 days and as needed with a start date on 12/21/24. During a record review of Resident 1's Medication Administration Record (MAR), dated 2/1/25 to 2/28/25, the MAR indicated that Resident 1's order for PICC line dressing change every 7 days was not provided by a Registered Nurse (RN). During an observation on 02/24/25 at 10:22 a.m. with Resident 1, Resident 1 was lying down in his bed and was observed to have a PICC line on his left upper arm. During an interview on 2/27/25 at 1:58 p.m. with the Director of Nursing (DON), the DON stated Resident 1 was admitted to the facility with PICC line even though Resident 1 was not on intravenous (through the vein) therapy. The DON stated Resident 1 had refused multiple times for his PICC line to be removed. The DON stated Resident 1 did not want the PICC line removed for future use. The DON stated she was responsible in changing the PICC line dressing. The DON stated Resident 1 had also refused PICC line dressing change multiple times. The DON stated the last dressing change she provided for Resident 1 was back in January 2025. During a concurrent record review and interview on 2/28/25 at 9:29 a.m. with the Assistant Director of Nursing (ADON), Resident 1's progress notes and care plan were reviewed. The ADON stated there were no documentations since admission that Resident 1 had been refusing to have his PICC line removed or have his PICC line dressing changed. The ADON stated there were also no records that the facility had monitored Resident 1 for complications of the PICC line. The ADON further they also did not conduct an Interdisciplinary Team (IDT, a team that includes staff members from multiple disciplines such as nursing, therapy, physicians, and other advanced practitioners) meetings that should have discussed the PICC line care for Resident 1.The ADON stated IDT meetings and care plans for PICC line care should have been developed when Resident 1 was admitted to the facility because Resident 1 was at risk for PICC line complications including infection. During a follow up interview on 2/28/25 at 9:32 a.m. with the DON, the DON stated she did not measure Resident 1's PICC line's external catheter length (helps ensure it stays in the correct position) and arm circumference (serves as a reference to determine any arm swelling should it occur due to complications from PICC placement) since Resident 1 was admitted . The DON stated she should have measured and documented Resident 1's external catheter length and arm circumference for monitoring and because it was the standards of practice. During a review of the facility's policy and procedure (P&P), titled Peripheral and Midline IV Dressing Change, dated March 2022, the P&P indicated, The purpose of this procedure is to prevent complications associated with IV therapy, including catheter-related infections associated with contaminated, loosened or soiled catheter-site dressings .Perform site care and dressing change at establisbhed intervals or immediately if the integrity of the peripheral dressing compromised .Change the dressing if it becomes damp, loosened or visibly soiled and .at least every 7 days for TSM (Transparent Semi-Permeable Membrane dressing) .measure arm circumference and compare to baseline when clinically indicated to assess for edema and possible deep vein thrombosis . During a review of the facility's P&P, titled, Charting and Documentation, dated July 2017, the P&P indicated, All services provided to the resident, progress toward the care plan goals, or any changes in the resident's medical, physical, functional or pyschosocial condition, shall be documented in the resident's medical record.The medical record should facilitate communication between the interdisciplinary team regarding the resident's condition and response to care .Documentation of procedures and treatments will include care-specific details, including .whether the resident refused the procedure/treatment .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Drug Regimen Review (Tag F0756)

Could have caused harm · This affected 1 resident

Based on interview and record review, for two of 15 sampled residents (Resident 3 and Resident 14), the facility failed to ensure; 1. An irregularity in Resident 14's medication regimen was identified...

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Based on interview and record review, for two of 15 sampled residents (Resident 3 and Resident 14), the facility failed to ensure; 1. An irregularity in Resident 14's medication regimen was identified by Consultant Pharmacist (CP) when fleet enema (laxative in the relief of occasional constipation, contains high levels of phosphates and sodium) was included in the bowel regimen despite Resident 14's constant refusal of phosphate binder. This failure had the potential to result in adverse events that included kidney injury. 2. Recommendation about Resident 3's medication regimen was not followed-through.This failure had the potential to result in increased risk of medication side effects. Findings: 1. During a review of Resident 14's admission Record (AR), the AR indicated Resident was initially admitted to the facility in September 2024 with diagnoses that included muscle weakness, difficulty walking and end stage renal disease (ESRD, the final stage of long-term kidney disease when the kidneys are no longer sufficiently able to remove waste products and excess water to support the body's needs). During a review of Resident 14's Order Summary Report dated 2/27/25, the Order Summary Report, indicated the following physician's orders; Milk of Magnesia (also called MOM, a laxative) suspension 400 milligrams (mg) per milliliters (ml) give 30 ml by mouth as needed for constipation if no bowel movement for two days. Fleet enema 7-19 grams (GM)/118 ml (sodium phosphates) insert one application rectally as needed if MOM and Dulcolax (another laxative) is ineffective and no bowel movement in eight hours. During a review of Resident 14's Medication Administration Record (MAR) for January 2025 and February 2025, the MAR indicated an order for Sevelamer HCL (hydrochloride, a medication that binds to phosphate in the digestive tract, preventing its absorption into the bloodstream thereby reducing the phosphate level) oral tablet 800 mg two tablets by mouth three times daily with meals. The January 2025 MAR indicated Resident 14 had repeatedly refused the medication. The February 2025 MAR indicated, on 2/26/25, the medication was discontinued after Resident 14 had refused 74 out of 76 doses of the phosphate binder. During an interview on 2/26/25 at 11:07 a.m. with Licensed Vocational Nurse (LVN) 1, LVN 1 stated Resident 14's bowel regimen for constipation was milk of magnesia, if that was not effective, to give Dulcolax suppository, and if the suppository still was not effective, to give fleet enema. LVN 1 stated it was safe to give the enema, one that has salt, sodium and phosphates because Resident 14 could just Easily flush it out anyway. During an interview and concurrent record review on 2/26/25 at 12:38 p.m. with Assistant Director of Nursing (ADON), ADON stated the facility's bowel regimen was a standing order for all residents but should have been changed for residents that were on dialysis (a treatment for kidney failure to remove waste products and excess fluids by external filtration of blood) because these residents should not be getting milk of magnesia and fleet enema. During a telephone interview on 2/26/25 at 1:23 p.m. with Consultant Pharmacist (CP), CP stated fleet enema and milk of magnesia are not medications of choice for Resident 14 because of the increased risk for kidney injury which could be critical for residents with kidney disease, especially that Resident 14 was not getting any phosphate binder. CP stated the medications should be discontinued. CP stated this could have been an irregularity in the medication regimen that was not identified during monthly medication regimen review. During a review of the facility's policy and procedure (P&P) titled Bowel Regimen for Renal Patients, undated, the P&P indicated due to fluid restrictions, dietary limitations and medication side effects, renal patients are at an increased risk for constipation, a bowel regimen to promote regular bowel movements and prevent complications will be implemented. The pharmacologic (the treatment of disease through the application of medications) management included the first line options such as stool softeners and second-line options include lactulose. The P&P indicated to avoid magnesium and phosphate-containing laxatives such as milk of magnesia and phosphate enemas as they increase the risk of electrolyte imbalance. 2. During a review of Resident 3's AR, the AR indicated Resident 3 was admitted to the facility in December 2023 with diagnoses that included muscle weakness, seizures, hypertension and osteoporosis, Resident 3 was on palliative care (hospice, specialized care focused on comfort, quality of life, and dignity for individuals with a terminal illness). During a review of Resident 3's Order Summary Report, the Order Summary Report indicated Resident 3 was discontinued from hospice and transitioned to custodial (long-term) care effective 11/11/24. The report also indicated an order for acetaminophen oral tablet 500 milligrams (mg) two tablets by mouth every six hours as needed for severe pain (7-10, total of 4,000 mg or 4 grams per day). During an interview and concurrent record review of Nursing Recommendations by CP on 2/26/25 at 12:29 p.m. with ADON, ADON stated Medication Regimen Review was done on 1/6/25 with recommendation to reduce daily dose of acetaminophen from 4 grams to 3 grams, which has not been communicated to the prescribing physician yet. During a telephone interview on 2/26/25 at 1:23 p.m. with CP, CP stated the facility has to be better responsive to MRR recommendations. CP stated she was still trying to catch up with recommendations that were made in the past months that have not been followed-through. During a review of the P&P titled Medication Regimen Reviews dated 2001, the P&P indicated, the consultant pharmacist provides a written report to the attending physician for each resident identified as having non-life threatening medication irregularity within 24 hours. The attending physician documents in the medical record that the irregularity has been reviewed and what action was taken to address it.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0757 (Tag F0757)

Could have caused harm · This affected 1 resident

Based on interview and record review, for one of five sampled residents (Resident 71) reviewed for unnecessary medications, the facility failed to ensure Resident 71 received apixaban (anticoagulant m...

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Based on interview and record review, for one of five sampled residents (Resident 71) reviewed for unnecessary medications, the facility failed to ensure Resident 71 received apixaban (anticoagulant medication that has black box warning) with adequate monitoring for adverse effects. This failure had the potential to result in undetected adverse effects from the medication. Definition: Black Box Warning (BBW) is the strongest warning that the FDA (Food and Drug Administration) requires, and signifies that medical studies indicate that the drug carries a significant risk of serious or even life-threatening adverse effects. Findings: During a review of Resident 71's admission Record (AR), the AR indicated, Resident 71 was admitted to the facility in January 2025 with diagnoses that included heart failure and atrial fibrillation (common heart rhythm disorder where the upper chambers of the heart [atria] beat irregularly and rapidly) and difficulty walking. During a review of Resident 71's Order Summary Report dated 2/27/25, the Order Summary Report indicated an order for apixaban oral tablet 2.5 milligrams (mg) give one tablet by mouth twice daily. During an interview and concurrent review on 2/26/25 at 12:49 p.m. with Assistant Director of Nursing (ADON), Resident 71's Medication Administration Record (MAR) for January 2025 and February 2025 were reviewed. ADON stated, because apixaban is a prescription medication that comes with a BBW, it should be monitored for adverse effects such as bleeding. ADON stated the MAR indicated monitoring for adverse effects was not done. During a review of the facility's policy and procedure (P&P) titled Policy: Black Box Warning, undated, the P&P indicated patients receiving BBW medications must be closely monitored per the FDA's safety recommendation. A review of the manufacturer's insert for apixaban indicated, premature discontinuation of apixaban increase the risk of thrombotic events (such as stroke) and spinal hematoma (a localized collection of blood outside of blood vessels), patients are monitored frequently for signs and symptoms of neurological impairment, if neurological compromise is noted, urgent treatment is necessary. Other warnings and precautions include bleeding that included intracranial (hemorrhagic stroke) and gastrointestinal (upper gastroinstestinal and lower GI-rectal bleeding). [Reference: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19a60552-374d-4b8b-a8ce-ceae252ea5ba#LINK_0c9c1e5e-b49a-4bfd-9bda-bfaae5121d81].
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0808 (Tag F0808)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to follow the food preference and therapeutic diet as ordered by the physician for one out of 20 sampled residents (Resident 10)...

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Based on observation, interview, and record review, the facility failed to follow the food preference and therapeutic diet as ordered by the physician for one out of 20 sampled residents (Resident 10). These failures had the potential to result in Resident 10 feeling disrespected and placed Resident 10 at risk for choking. Findings: During a review of Resident 10's admission Record, printed 2/27/25, the record indicated Resident 10 was admitted to the facility in November 2023 with a diagnoses of low back pain and chronic obstructive pulmonary disease (COPD, refers to a group of diseases that cause airflow blockage and breathing-related problems. It includes emphysema and chronic bronchitis.) During a record review of Resident 10's undated Breakfast Meal Ticket, the meal ticket indicated Resident 10's diet was controlled carbohydrates (a diet that is designed to manage blood sugar levels) diet with mechanical soft texture (consist of soft, easily chewed and swallowed foods). The meal ticket also indicated Dislikes: Cereal, ravioli, cranberry juice, sausage . and Beverages: 2 milks. During a concurrent observation and interview on 2/26/25 at 9:25 a.m. with Resident 10, Resident 10 was having breakfast in her bed. Resident 10 was served hash browns, cream of wheat, a bowl of dry corn flakes cereal, and 2 small glasses of milk. Resident 10 stated she did not like the corn flakes because it was hard for her to chew, and she could have choked if she ate it. Resident 10 stated she was on a mechanical soft diet because her dentures could not bite and chew hard foods. Resident 10 stated she felt disregarded because her food preferences and therapeutic diet were not being followed by the facility. During an interview on 2/26/25 at 9:31 a.m. with the Certified Nursing Assistant (CNA) 1, CNA 1 stated Resident 10 notified her that she was given a bowl of dry cornflakes that she did not like to eat it. CNA 1 stated Resident 10 was also not provided a carton 1of milk for cereal CNA 1 stated the kitchen staff made a mistake and gave Resident 10 the wrong cereal. CNA 1 stated Resident 10 should have been given the correct therapeutic diet to prevent choking. During an interview on 2/26/25 at 10:33 a.m. with Dietary Manager (DM), DM stated the dry corn flakes cereal was provided to Resident 10 even though in the meal ticket indicated she was on mechanical soft diet and disliked cereal because Resident 10 had so many food preferences and it changed every now and then. DM stated the kitchen staff provided the dry corn flakes to Resident 10 because CNA 1 requested it. During an interview on 2/26/25 at 1:22 p.m. with the Director of Nursing, the DON stated the meal tickets should have been checked before serving the breakfast to Resident 10. The DON stated kitchen staff and CNA 1 should have respected and followed Resident 10's therapeutic diet and food preference. The DON stated no matter how long CNA 1 have known Resident 10; CNA 1 should have should have verified with a licensed nurse if Resident 10 was allowed to have dry corn flakes cereal to prevent issues like feeling upset and disrespected. During a record review of the facility's policy and procedure (P&P), titled, Therapeutic Diets, dated 2001, the P&P indicated, Therapeutic diets are prescribed by the attending physician to support the resident's treatment and plan of care and in accordance with his or her goals and preferences .Diet will be determined in accordance with the resident's informed choices, preferences, treatment goals and wishes.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure infection prevention and control practices whe...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure infection prevention and control practices when following was noted: 1. Seven (7) out of seven expired Intravenous Administration sets (IV kit, a medical device used to deliver nutrients and medications in a fluid form directly into patient's bloodstream) were kept in the medication storage room. 2. One (1) out of one expired Peripherally Inserted Central Catheter (PICC, a long, flexible thin tube, also known as catheter, put into a vein in upper arm for extended use) stabilizing device (a device to stabilize the wings of PICC line) were kept with ready to use medication administration supplies. This failure placed facility residents at risk for receiving medications via expired and with compromised sterility IV/ PICC line devices. Findings: During an observation and concurrent interview on [DATE] at 10:00 a.m. with Licensed Vocational Nurse (LVN 1), in facility's medication storage room, seven IV Kits with expiration date of [DATE], and one PICC line stabilizing device with expiration date of [DATE], were kept in the room along with other ready to use supplies. LVN 1 stated there were no unexpired IV kits and/or PICC line stabilizing device available at the facility. LVN 1 stated facility had one active resident in the facility at that time, who could have required above supplies. During an interview on [DATE] at 10:20 a.m. with the Director of Nursing (DON), DON stated it was important to discard expired medication administration supplies to maintain sterility. The DON stated night shift licensed nurses, and the DON were responsible to complete monthly audit to check entire medication storage room to ensure expired items were not kept. During an interview and record review on [DATE] at 10:25 a.m. with DON in medication storage room, a notice was posted in the medication room. The DON stated the notice indicated Night Shift Nurse's Responsibilities, which included change PICC Line/Central lines/IV dressing .change all tubings with date .check audit binder everyday. The DON stated, however, she was unable to find the documentation if facility was completing the medication room audits to ensure the integrity of all medication administration supplies.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. During a review of Resident 14's admission Record (AR), the AR indicated, Resident 14 was initially admitted to the facility ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. During a review of Resident 14's admission Record (AR), the AR indicated, Resident 14 was initially admitted to the facility in September 2024 with diagnoses that included muscle weakness, difficulty walking and end stage renal disease (ESRD, the final stage of long-term kidney disease when the kidneys are no longer sufficiently able to remove waste products and excess water to support the body's needs). During a review of Resident 14's Minimum Data Set (MDS, an assessment tool used to direct resident care) dated 10/20/24, the MDS indicated Resident 14 had moderate difficulty hearing (speaker has to increase volume and speak distinctly). Resident 14's most recent MDS dated [DATE] also indicated moderate difficulty hearing and a Brief Interview for Mental Status (BIMS, a scoring system to determine the resident's cognitive status in regard to attention, orientation, and ability to register and recall information) score of 14. A score of 13-15 is an indication of intact cognitive status. During an interview and concurrent review of Resident 14's comprehensive care plan on 2/26/25 at 9:35 a.m. with ADON, ADON stated Resident 14 had already been hard of hearing since being admitted from an independent living facility, but the personal inventory effects did not indicate Resident 14 was admitted with hearing aids. ADON stated a comprehensive care plan was not initiated to address inability to hear especially that the MDS already indicated Resident 14 had moderate difficulty hearing. During an interview and concurrent record review on 2/26/25 at 9:44 a.m. with Social Services Director (SSD), SSD stated Resident 14 was admitted to the facility for long term stay. SSD stated Resident 14 was sent to the hospital and returned to the facility with moderate difficulty in hearing. SSD also stated having to write on a piece of paper when communicating with Resident 14. SSD stated she did not know whether Resident 14 had a hearing aid while at the independent living facility and had not followed up if Resident 14's insurance could pay for hearing aid. SSD stated Resident 14 was admitted in September 2024 with adequate hearing but after Resident 14 went to the hospital and returned in October 2024, Resident 14 had been hard of hearing. SSD stated having told the DON about the change but could not show documentation that it was discussed with Nursing Department. SSD stated the normal process was for Nursing to flush the resident's ear to make sure there were no foreign objects in the ear, inform the doctor and the resident's responsible party, and set up appointment with audiology doctor. SSD stated none of these was done for Resident 14. During an interview on 2/26/25 at 10:03 a.m. with Certified Nursing Assistant (CNA) 1, CNA 1 stated she had to speak loudly into Resident 14's right ear during care. During an observation and concurrent interview on 2/26/25 at 10:05 a.m. with Resident 14, while in the activity room, Resident 14 stated it was bothersome that she could not have normal conversation where people did not have to be within inches from her face. Resident 14 was staring at the TV but said it was not loud enough. Based on observation, interview, and record review, the facility failed to develop and implement a comprehensive, person-centered care plan and meet the needs of three of three sampled residents (Resident 1, 9 and 14) when: 1. The facility did not develop a care plan to address Resident 1's peripherally inserted central catheter (PICC, a tube used to deliver medications and other treatments directly to the large central veins near the heart) care. 2. The facility did not develop a care plan to address Resident 9's weight loss of 2.4lbs (pounds) in one week due to very low food and fluid intake. 3. The facility did not develop a care plan to address Resident 14's hearing loss. These failures had the potential to result in Residents 1, 9, and 14 not receiving appropriate care, monitoring, and treatment. Findings: 1. During a record review of Resident 1's admission Record', printed on 2/27/25, the admission Record indicated Resident 1 was admitted to the facility in December 2024 with diagnosis of cellulitis (bacterial skin infection) of right and left lower limbs. During an observation on 02/24/25 at 10:22 a.m. with Resident 1, Resident 1 was lying in his bed and was observed to have a PICC line on his left upper arm. During an interview on 2/27/25 at 1:58 p.m. with the Director of Nursing (DON), the DON stated Resident 1 was admitted to the facility with a PICC line on left upper arm. The DON stated Resident 1 was not on any intravenous (through the vein) therapy. The DON stated Resident 1 had history of refusals for his PICC line to be removed or the dressing to be changed since Resident 1 was admitted to the facility. The DON stated Resident 1 wanted to keep his PICC line for future use. The DON stated the last dressing change she provided for Resident 1 was back in January 2025. During a concurrent record review and interview on 2/28/25 at 9:29 a.m. with the Assistant Director of Nursing (ADON), Resident 1's progress notes and care plan were reviewed. The ADON stated they did not create a comprehensive care plan and there was also no Interdisciplinary Team (IDT, a team that includes staff members from multiple disciplines such as nursing, therapy, physicians, and other advanced practitioners.) meetings that addressed Resident 1's PICC line care when Resident 1 was admitted to the facility. The ADON futher stated there were also no documentations from the licensed nurses that Resident 1 been refusing the PICC line removal or PICC line dressing change. The ADON stated a care plan and IDT should have been developed because it was important to monitor Resident 1's PICC line for any complications including infection on the PICC line site. During a record review of the facility's policy and procedure (P&P), titled, Care Plans, Comprehensive Person-Centered, dated March 2022, the P&P indicated, A comprehensive, person-centered care plan that includes measurable objectives and timetables to meet the resident's physical, psychosocial and functional needs is developed and implemented for each resident .The interdisciplinary team in conjunction with the resident and his/her family or legal representative, develops and implements a comprehensive, person-centered care plan for each resident .The comprehensive, person centered care plan describes the services that are to be furnished to attain or maintain the resident's highest practicable physical, mental, and psychosocial well-being, including services that would otherwise be provided for the above, but are not provided due to the resident exercising his or her rights, including the right to refuse treatment . 2. During a record review of Resident 9' admission Record', printed on 2/27/25, the admission Record indicated Resident 9 was admitted to the facility in February 2025 with multiple diagnoses including urinary tract infection (an infection of the urinary tract, which includes the kidneys, ureters, bladder, and urethra) and Parkinson's disease (a brain disorder that causes unintended or uncontrollable movements, such as shaking, stiffness, and difficulty with balance and coordination. Symptoms usually begin gradually and worsen over time. As the disease progresses, people may have difficulty walking and talking. They may also have mental and behavioral changes, sleep problems, depression, memory difficulties, and fatigue.) During a record review of the Registered Dietician's (RD) Progress Notes, dated 2/18/25, the Progress Notes indicated, Resident 9 had a notable weight loss of 2.4lbs in one week likley due to very low PO (by mouth) intake. The RD's progress notes indicated Resident 9 was only consuming 0-25% of her meals and it was not enough to meet Resident 9's needs. During an interview on 2/26/25 at 11:12 a.m. with Licensed Vocational Nurse (LVN) 2, LVN 2 stated Resident 9 needed another person to feed and encourage her during meal times because Resident 9 did not eat and drink very well. During an interview on 2/28/25 at 10:31 a.m. with the ADON, ADON stated Resident 9's weights should have been monitored upon admission and every week. ADON also stated when Resident 9 was admitted , they were aware that Resident 9 was high risk for malnutrition and weight loss due poor eating and drinking habit. ADON stated she did not know that Resident 9 had an actual weight loss of 2.4lbs in one week. ADON further stated they did not have any IDT meetings and they did not develop a care plan to address Resident 9's very low PO intake and weight loss. ADON stated they should have developed a comprehensive care plan for Resident 9 to monitor if the goals in resolving weight loss and was being met by the facility. During a record review of the facility's P&P, titled, Weight Assessment and Intervention, dated March 2022, the P&P indicated, 1. Care planning of weight loss or impaired nutrition is multidisciplinary effort and include the physician, nursing staff, the dietician, the consultant pharmacist, and the resident or the resident's legal surrogate . 2. Individualized care plans shall address to extent possible .a. identified cause of weight loss .b. goals and benchmarks for improvement .c. time frames and parameters for monitoring and reassessment.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected multiple residents

Based on observation, interview and record review, the facility failed to ensure medication rate was five (5) percent or less when three medication errors were observed out of 25 opportunities (medica...

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Based on observation, interview and record review, the facility failed to ensure medication rate was five (5) percent or less when three medication errors were observed out of 25 opportunities (medication error rate was calculated as followed: three divided by 25 then multiplied by 100, which was equal to 12 percent) when: 1.Resident 71 did not receive snack/food with Metformin (an oral medication to control blood glucose in the blood) tablet. 2.Licensed Nurse did not instruct Resident 12 to press inner canthus (inner corner of the eye where the upper and lower eyelids meet) after administering eye drops. 3.Licensed Nurse did not check Resident 5's Vital Signs (measurements of the body's most basic functions, including heart rate, pulse, temperature, respirations) before, during, and/or after nebulizer treatment. These failures placed Resident 71, Resident 12, and Resident 5 at risk for ineffective/compromised effects of above-mentioned medications. Findings: 1. A review of Resident 71's physician order dated 1/21/25, indicated to give one tablet of Metformin HCl) 850 milligrams (mg) by mouth two times a day for Diabetes Mellitus Type II (a long-term condition in which the body has trouble controlling blood sugar and using it for energy). During an observation on 2/25/25 at 9:48 a.m. Licensed Vocational Nurse (LVN) 1 did not provide a snack or meal with administration of Metformin 850 mg oral tablet to Resident 71. During an interview on 2/25/25 at 01:59 p.m. with LVN 1, LVN 1 stated she gave Metformin without food because breakfast was at 0730 and lunch was at 1130-1200. LVN 1 stated it was important to give snacks/food with Metformin tablets to Resident 71 because, it could upset Resident 71's stomach. A review of manufacturer's guidelines for Metformin hydrochloride; and Metformin Extended- Release tablets dated 04/2017 indicated, it should be given once daily with the evening meal. 2. During a record review of Resident 12's Physician order dated 9/3/22, indicated to administer one drop of Artificial tears solution 1% (Carboxymethylcellulose Sodium; eye drop protectant against further irritation or to relieve dryness of the eye) in both eyes two times a day for eye dryness. During an observation on 2/25/25 at 9:38 a.m. Licensed Vocational Nurse (LVN) 2 instructed Resident 12 to rapidly blink eyes after administration of Artificial tears eye drops. During an interview on 2/25/25 at 02:11 p.m. with LVN2, LVN 2 stated, I should have followed the standard nursing practice to instruct Resident 12 to slowly close eyes and press inner canthus (inner corner of the eye where the upper and lower eyelids meet) for absorption of eye medication. During a record review of facility's undated Policy and Procedure (P&P) titled 'Instillation of Eye Drops' the P&P indicated instruct the resident to slowly close his/her eyelid to allow for even distribution of the drops. Instruct the resident not to blink or squeeze the eyelids shut, which forces the medication out of the eye. 3. During a record review of Resident 5's Physician order dated 3/7/24, the order indicated to administer Ipratropium-Albuterol (inhaled solution used to help control the symptoms of lung disease) Inhalation Solution 0.5-2.5 3 milligrams/3 milliliters (mg/ml) (Ipratropium-Albuterol; s) During an observation on 2/25/25 at 01:41 p.m. with LVN2, LVN 2 did not check Resident 5's vital signs (measurements of the body's most basic functions, including heart rate, pulse, temperature, respirations) before, during or after inhalation treatment. During an interview on 2/26/25 at 09:26 a.m. with LVN2, LVN 2 stated it was important to check Resident 5's vital signs routinely during treatment to see if medication was working. During a record review of facility's undated P&P titled 'Administering Medications through a Small Volume (Handheld) Nebulizer the P&P indicated, obtain baseline pulse, respiratory rate, and lung sounds .approximately five minutes after treatment begins obtain the residents pulse .obtain post-treatment pulse, respiratory rate and lung sounds .
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observation, interview and record review, the facility failed to prepare food in accordance with professional standards of food service safety when: -Frozen meats inside the refrigerator were...

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Based on observation, interview and record review, the facility failed to prepare food in accordance with professional standards of food service safety when: -Frozen meats inside the refrigerator were thawed on top of ready-to-drink fresh milk. -Multiple kitchen staff used the wrong test strip to check sanitizer concentration for the three-compartment sink and dishwasher. -Frozen chicken was thawed on the food preparation counter before cooking. -Two kitchen staff did not wear hair cover during food preparation. These failures had the potential to result in cross-contamination and food-borne illnesses. Findings: During an observation and concurrent interview on 2/24/25 at 10:22 a.m. with Dietary Manager (DM), inside the reach-in refrigerator, the following were observed: a) A pan overflowing with chicken and turkey, thawing on top of multiple gallons of fresh milk. DM stated there was not enough space in the refrigerator, so the staff had to somehow squeeze the meats in. b) DM tested the three-compartment sink sanitizer concentration by submerging two inches of the test strip in the solution and obtained a reading of 50 ppm (parts per million, unit used to describe very small concentrations of a substance in a larger solution). An instruction on how to check for quaternary (quat, a group of chemicals used in many products, including disinfectants, sanitizers, and detergents) sanitizer was posted on the wall above the three-compartment sink. DM stated the facility has stopped using quat sanitizer for a while now but forgot to remove the signage. Review of the poster titled Quat Sanitizer Testing Procedures indicated the following: sanitizer solution must be clean and between 200-400 ppm concentration, solution must be at room temperature, submerge test paper in solution and hold still for 10 seconds, and compared to chart on the test paper immediately, reading should be between 200-400 ppm concentration. c)DM stated the dishwasher sanitizer concentration was checked with Spartan pH test strip with a pH (a measure of how acidic/basic water is) of 10. During a follow-up observation and concurrent interviews with multiple kitchen staff on 2/27/25 between 9:36 a.m. and 9:50 a.m., [NAME] 2 prepared pureed turkey at the food preparation area. [NAME] 2 wore a hat that did not completely cover his hair from above the ears to the nape area. There were pieces of frozen chicken thighs submerged in clear liquid inside a plastic bowl placed on the food preparation counter. Kitchen Staff (KS) stated the frozen chicken were pulled from the freezer at 9:30 a.m. and was thawed for lunch service. During an observation and concurrent interviews on 2/27/25 at 9:54 a.m. with KS and [NAME] 1, KS used Spartan pH test strip by submerging the strip in a pool of rinse water in the dishwasher for three seconds. KS stated the test strip came back with a pH 9 reading. KS stated the pH level should be 102, then proceeded to write 100 under breakfast test strip for 2/25/25 in the Dish Machine Temperature Log. KS stated 100 meant 100% but unable to explain further. KS did not answer why there were missing temperature logs for 2/25/25 and 2/26/25, or why he recorded the day's sanitizer and temperature level under 2/25/25. [NAME] 1 stated 100 meant 100 ppm but failed to show how he came up with 100 ppm since the chart on the test strip only showed 1-14 pH. Both KS and [NAME] 1 stated they had only used the pH strip to check dishwasher sanitizer level. During review of the Dish Machine Temperature Log (Low Temp Machine) for February 2025, for 2/1/25 to 2/25/25, test strip readings were all 100 for breakfast, lunch and dinner. During another observation and concurrent interviews on 2/27/25 at 10:10 a.m. with KS and [NAME] 1 to check the three-compartment sink sanitizer concentration, KS stated using the Hydrion Chlorine test strip but failed to explain how it was done. [NAME] 1 stated to submerge the test strip in a bucket of the sanitizer solution for 30 seconds and compare the color of the test strip with the color chart on the box. The test strip came back white (unchanged) but [NAME] 1 stated the reading was 50 ppm. [NAME] 1 submerged another strip which turned into mottled purplish gray, which he stated was 100 ppm. During a telephone interview on 2/27/25 at 10:15 a.m. with Vendor 1, Vendor 1 stated, for the dishwasher, the pH test strip was to check the detergent concentration while the chlorine test strip would check for the sanitizer concentration. Vendor 1 also stated, for the three-compartment sink, quat sanitizer was used so a quat test strip, not the chlorine test strip, should be used by staff to check for sanitizer level. During a review of the Quaternary Ammonium Log for February 2025, that had been scratched off with multiple lines across and was replaced by Sanitizer. The instructions included to test the ammonium concentration in the quaternary sanitizer per policy using the proper strips, Ammonium reading should be at least 200 ppm or manufacturer's recommendation, crossed out with a line across and replaced with 50-100 ppm. Record reading once in the morning and once in the afternoon. The log indicated one test strip reading daily. During an observation and concurrent interview on 2/27/25 at 10:37 a.m. with DM, DM stated staff should use the chorine test strip to check sanitizer concentration for the three-compartment sink. [NAME] 2 was observed cooking the previously frozen chicken thighs that were thawing on the counter for an hour. DM stated, frozen food, when thawed as part of the cooking process, As long as it is cooked right away, it is okay. During a review of the facility's policy and procedure (P&P) titled Thawing of Meats dated 2023, the P&P indicated thawing meat can be done; in a refrigerator on the bottom shelf below prepared, ready-to-eat foods, submerge under running, potable water with a pressure sufficient to flush away loose particles, and as part of the cooking process, works well with frozen vegetables and ground meat. During an observation on 2/28/25 at 9:23 a.m., DM was at the food preparation counter preparing salads for lunch service, not wearing hair cover. During a review of the facility's P&P titled Dress Code dated 2023, the P&P indicated for kitchen staff to wear hat for short hair, the hat should completely cover the hair, or hair net when hair is over the ear or longer.
Dec 2024 1 deficiency
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Medication Errors (Tag F0758)

Could have caused harm · This affected 1 resident

Based on interview, record review, and facility policy review, the facility failed to ensure one (Resident 1) of three sampled residents was free from unnecessary drugs when facility's interdisciplina...

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Based on interview, record review, and facility policy review, the facility failed to ensure one (Resident 1) of three sampled residents was free from unnecessary drugs when facility's interdisciplinary team (IDT) did not re-evaluate use of Seroquel (an antipsychotic medication) at the time of admission and/ or within two weeks for its appropriateness and indication for use to consider whether or not the medication could be reduced, tapered, or discontinued. Interdisciplinary team is a group of healthcare professionals who work together to treat a patient condition. This failure had the potential for Resident 1 to receive unnecessary medications and placed her at risk to suffer adverse effects from the medication. Findings: During a review of Resident 1's admission Record (AR), dated 12/23/24, the AR indicated, Resident 1 was admitted from acute care hospital on 8/22/24. During a review of Resident 1's Admission-Minimum Data Set (MDS- Resident Assessment and care guide tool) dated 8/26/24, the MDS indicated Resident 1 had no potential indicators of psychosis e.g., hallucinations (perceptual experiences in the absence of real external sensory stimuli) or delusions (misconceptions or beliefs that are firmly held, contrary to reality). MDS indicated Resident 1 had no physical or verbal behavioral symptoms directed towards others e.g., verbal/vocal symptoms like screaming or disruptive sounds, hitting, kicking, pushing, scratching, or grabbing at others. MDS indicated Resident 1's diagnosis included chronic obstructive pulmonary disease with acute exacerbation (COPD-a worsening group of lung diseases that block airflow and make it difficult to breathe). During a review of Resident 1's Order Summary Report dated 8/22/24, indicated the physician prescribed Resident 1 Seroquel oral tablet 25 mg give one tablet by mouth at bedtime for mood disorder manifested by yelling and hitting for 14 days. Further review of Resident 1's Order Summary Reports dated 9/3/24 and 9/18/24, indicated physician continued prescribing Resident 1 Seroquel oral tablet 25 mg, to give one tablet by mouth at bedtime for mood disorder manifested by yelling and screaming. During a review of Resident 1's Medication Administration Record (MAR), dated 8/23/24 to 8/31/24 and 9/1/24 to 9/18/24, the MARs indicated Resident 1 was administered Seroquel 25 mg give one tablet by mouth at bedtime for yelling, hitting and screaming. During an interview on 12/23/24 at 11:17 a.m. with Certified Nursing Assistant (CNA) 1, CNA1 stated CNA1 cared for Resident 1 four days a week. CNA1 stated Resident 1 had behavior of calling out for help from time to time. CNA1 stated when Resident 1 was asked what she needed, Resident 1 said nothing. During an interview on 12/27/24 at 11:29 a.m. with Licensed Vocational Nurse (LVN 1), LVN 1 stated Resident 1 was prescribed Seroquel from Resident 1 stay at the hospital. LVN 1 stated Resident 1 had COPD, was on oxygen therapy. LVN 1 stated Resident 1 had anxiety behavior when she had problem with breathing and inability to relax; she would call out for help. During an interview on 12/27/24 at 11:37 a.m. Licensed Vocational Nurse (LVN 2), LVN 2 stated Resident 1 was nice and cooperative. LVN 2 stated Resident 1 sometimes had anxiety and called out for help. During a review of Resident 1's Consultant Pharmacist's Medication Regimen Review (MRR), dated 8/27/24, the MRR indicated, Resident 1 had an order for Seroquel 25 mg at bedtime for 14 days. If the drug is to be continued beyond its initial 14-day period, you may wish to ask if the dose could be reduced to 12.5 mg at bedtime . mood disorder is not a usual diagnosis for an antipsychotic, If continued beyond 14 days please clarify diagnosis . During a concurrent interview and record review on 12/31/24 at 10:16 a.m. with the Director of Nursing (DON), Resident 1's progress notes, care plan use of antipsychotic, MRR dated 8/27/24 and facility's policy and procedure (P&P) titled, Antipsychotic Medication Use were reviewed. The DON stated facility did not reevaluate Resident 1's use of Seroquel medication at the time of admission or within two weeks of her admission to the facility, to consider reduction or discontinuation. The DON stated she was unable to find documentation if facility followed up on pharmacist's recommendations made on 8/27/24. During a review of the facility's policy and procedure (P&P) titled, Antipsychotic Medication Use, revised July 2022, the P&P indicated, Residents who are admitted from the community or transferred from a hospital and who are already receiving antipsychotic medications will be evaluated for the appropriateness and indications for use. The interdisciplinary team will re-evaluate the use of the antipsychotic medication at the time of admission and / or within two weeks (at the initial MDS assessment) to consider whether or not the medication can be reduced, tapered, discontinued.
Oct 2023 8 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Resident Rights (Tag F0550)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to serve puree meals on plates (they were served in cups...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to serve puree meals on plates (they were served in cups) for two residents (Resident 3 and Resident 120) out of 12 sampled residents. This failure had the potential to cause residents, who are on altered textures to lose their rights to be treated with dignity. Findings: During a review of Resident 3's admission Record, the admission Record indicated, admission of date of 3/25/23 with diagnoses including Other sequelae of cerebral infarction (residual effects after a stroke). During a review of Resident 120's admission Record, the admission Record indicated, admission date of 10/9/23 with diagnoses including Encounter for Palliative care (comfort care for terminally ill residents) and dysphagia (trouble swallowing). During a review of Resident 3's Physician Orders, dated 10/2023, the Physician Orders indicated, Resident 3 is on regular diet, puree texture, and thin liquids. During a review of Resident 120's Physician Orders, dated 10/2023, the Physician Orders indicated Resident 120 was on regular diet, pureed texture, nectar consistency. During a review of Resident 3's Minimum Data Set (MDS - an assessment used to guide plan of care), dated 8/29/23, the MDS indicated a Brief Interview for Mental Status (BIMS - an assessment to measure cognition) score of 2 indicating severe cognitive impairment. During a review of Resident 120's MDS, dated [DATE], the MDS did not have a BIMS score. MDS further indicated that resident is rarely/never understood. During a concurrent observation and interview on 10/17/23 at 11:51 a.m., with Kitchen Supervisor (KS) in the kitchen, puree food was observed in individual thick, red, plastic bowls. KS stated, that puree foods are always served in individual cups because it is easier for residents to scoop. During an observation on 10/17/23 at 12:31 p.m. in Resident 120's room, Resident 120's food tray had 3 individual thick red cups containing pureed food. During an observation on 10/17/23 at 12:32 p.m., in Resident 3's room, Resident 3's lunch tray had 3 individual thick red cups containing pureed food. During a record review on 10/19/23 at 1:11 p.m., of Resident 120 's electronic health record, the record indicate no assessments nor progress notes addressing preference for meals to be served in individual cups. A subsequent record review of Resident 3's health record also did not have assessments nor progress notes indicating a preference for meals to be served in individual cups. During an interview on 10/18/23 at 9:30 a.m., with Registered Dietician (RD), RD states that puree food needs to be served on a plate or else it can be a dignity issue. During a review of the facility's policy and procedure titled Resident Rights (undated), indicated residents have a right to .a. a dignified existence, b. be treated with .dignity .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to follow physician orders when administering oxygen to one resident (Resident 170) out of 12 sampled residents. This failure ha...

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Based on observation, interview, and record review, the facility failed to follow physician orders when administering oxygen to one resident (Resident 170) out of 12 sampled residents. This failure has the potential to cause Resident 170 to be given too much oxygen, which could result in hospitalization. Findings: During a review of Resident 170's admission Record, the admission Record indicated a readmission date of 7/26/23 with diagnosis including Chronic Obstructive Pulmonary Disease (COPD - a lung disease that blocks airflow and makes it difficult to breathe). During an observation on 10/16/23 at 9:12 a.m., in Resident 170's room, Resident 170 was asleep with oxygen via nasal cannula (a device used to deliver supplemental oxygen) at 2.5L/min. During a follow up observation and interview on 10/18/23 at 10:54 a.m., with Resident 170, inside Resident 170's room, Resident 170 was observed with nasal cannula and supplemental oxygen was delivered at 2.5L/min. Resident 170 stated, he uses oxygen mostly at night. During a concurrent record review and interview on 10/18/23 at 10:55 a.m., with Licensed Vocational Nurse (LVN 1), Resident 170's physician orders dated 10/2023 and progress notes were reviewed. The physician orders indicated O2 @ 1L/min via NC to keep oxygen saturation >94% as needed. LVN 1 stated, resident 170 was having difficulty breathing yesterday (10/17) so she bumped up oxygen' to 2-3 (liters). LVN 1 also stated, that for any change of condition, there should be an SBAR (Situation, Background, Assessment, Recommendation - a way to clearly and concisely communicate a resident's situation), notify MD, and write progress notes. A review of Resident 170's progress notes did not show change of condition documentation and no SBAR documentation. During a record review of Resident 170's nursing progress notes from 8/2023 to 10/2023, nursing progress notes indicated Resident 170, was on supplemental oxygen at 2 liters per minute starting 10/2/23 through last progress note dated 10/9/23. A nursing progress note dated 8/10/2023 indicated a new order for oxygen to be given 1L/min via NC to keep oxygen saturation >94% as needed. During an interview on 10/19/23 at 9:09 a.m., with Director of Nursing (DON), DON stated if resident 170 is having difficulty breathing, put 1 liter of oxygen as ordered, if it is not enough, then turn up the oxygen until 3L until oxygen saturation is in acceptable range, then notify MD they had to change the amount of oxygen. Nurses will then document in skilled charting or progress note. DON stated that if there is a need to change orders, then nurses need to do SBAR and change of condition (COC) charting.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0698 (Tag F0698)

Could have caused harm · This affected 1 resident

Based on interview, and record review, the facility failed to ensure dialysis (a treatment to remove extra fluid and waste products from the blood when the kidneys cannot) communication records were c...

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Based on interview, and record review, the facility failed to ensure dialysis (a treatment to remove extra fluid and waste products from the blood when the kidneys cannot) communication records were completed for one (Resident 6) of one sampled resident. This failure had the potential to miss signs of illness such as fever or bleeding, which could lead to hospitalization. Findings: A review of Resident 6s admission record, the admission record indicated, admission date of 7/23/23 with diagnoses including end stage renal disease (the last stage of long-term kidney disease where the kidneys no longer work) and dependence on renal dialysis. During a review of Resident 6's Order Summary Report, the Order Summary Report indicated, Resident 6 had dialysis three times a week on Tuesdays, Thursdays, and Saturdays. During a record review of Resident 6's Hemodialysis Communication records dated 9/12/23 through 10/17/23, the Hemodialysis Communication records for hemodialysis treatment days on 9/12/23, 10/7/23 and 19/17/23 were not completed. During a concurrent interview and record review, on 10/18/23 at 8:51 a.m., of Resident 6's Hemodialysis Communication records, dated 9/12/23, 10/7/23, and 10/17/23, with Director of Staff Development (DSD), DSD confirmed Hemodialysis Communication records were missing. DSD further stated, it is important to check resident after treatment to monitor bleeding from the access site and check for signs of infection. DSD stated, it is important because staff need to know what is going on with the resident and they are expected to complete the hemodialysis communication record before the resident goes to dialysis and when the resident returns to facility. During a review of the facility's policy and procedure titled, Care of a Resident on Dialysis (undated), the policy indicated nursing services .monitor and assess the resident's condition, the effects of dialysis and .prevent complications .5.Nursing must complete dialysis communication form on dialysis days .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility gave Insulin Aspart (a drug used to treat diabetes; a condition ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility gave Insulin Aspart (a drug used to treat diabetes; a condition that develops when a person's blood sugar is too high) 2 units, late to one (Resident 10) of 10 sampled residents. This failure resulted in Resident 10 not receiving medication as prescribed by the physician and placed Resident 10's health at risk due to risk of a negative effect on Resident 10s blood sugar. Findings: During a review of Resident 10's admission Record (AR), dated 10/19/23, the AR indicated Resident 10 was admitted to the facility on [DATE], and had a diagnosis of Diabetes Mellitus (a condition that develops when a person's blood sugar is too high). During an observation on 10/17/23 at 2:12 p.m., Licensed Vocational Nurse (LVN) 1 was observed giving the medication, Insulin Aspart 2 units, to Resident 10. During a concurrent interview and record review on 10/17/23 at 2:15 p.m., with LVN 1, Resident 10's Medication Administration Record (MAR) was reviewed. The MAR indicated, Insulin Aspart Injection Solution . inject as per sliding scale if 70 - 150 = No insulin . 151-200 = 2 units 201 - 250 = 3 units, 251 - 300 = 4 units . before meals and at bedtime for DM (DM - Diabetes Mellitus). LVN 1 stated, she checked Resident 10's blood sugar at 11:00 a.m. LVN 1 stated, the blood sugar was 166, and per the sliding scale she needed to give 2 units to Resident 10. LVN 1 stated, Resident 10 ate his lunch around noon. LVN 1 stated, she usually gave Resident 10 the insulin between 11:00 a.m. and 11:30 a.m. LVN 1 stated, she gave the insulin after lunch because Resident 10 was in the physical therapy room before lunch and she couldn't give the medication to him there. LVN 1 stated, she had not checked the blood sugar again after 11:00 a.m. During a review of Resident 10's Order Summary Report (ORD), dated 10/19/23, ORD indicated, Resident 10 was ordered Insulin Aspart Injection Solution . inject as per sliding scale if 70 - 150 = No insulin . 151-200 = 2 units 201 - 250 = 3 units, 251 - 300 = 4 units . before meals and at bedtime for DM (DM - Diabetes Mellitus). During a review of Resident 10's Insulin Aspart Injection Solution 100 UNIT/ML (Insulin Aspart) Administration History (ADH), dated 10/19/23, the ADH indicated, Resident 10 was given 2 Units of Insulin Aspart by LVN 1 on 10/17/23 at 2:12 p.m. During an interview on 10/18/23 at 3:35 p.m., with Director of Nursing (DON), DON stated, Resident 10's Insulin Aspart should have been given before lunch, as it is ordered to be given before lunch. DON stated, giving the Insulin Aspart after lunch was an error and could have negatively affected the resident's blood sugar and health. During an interview on 10/19/23 at 12:15 p.m., with the Director of Staff Development (DSD), DSD stated, LVN 1 should have given Resident 10 Insulin Aspart before lunch as ordered by the doctor. DSD stated, LVN 1 should have removed Resident 10 from the physical therapy room, given Resident the Insulin Aspart, and returned Resident 10 to the physical therapy room. DSD stated, when LVN 1 gave the Insulin Aspart late, Resident 10's blood sugar and health were at risk of a negative effect. During a review of the facility's policy and procedure titled, Administering Medication, undated, indicated . 3. Medications must be administered in accordance with the orders, including any required time frame.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure staff followed the infection control program de...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure staff followed the infection control program designed to prevent the spread of infection for one of 10 sampled residents (Resident 10) when Licensed Vocational Nurse (LVN) 1 failed to perform hand hygiene after removing gloves, LVN 1 had put on to give eye drops. This failure had the potential to cause infection or spread infection. Findings: During a review of Resident 10's admission Record (AR), dated 10/19/23, the AR indicated Resident 10 was originally admitted to the facility on [DATE]. During an observation on 10/17/23 at 1:18 p.m., in Resident 10's room, LVN 1 put on gloves. LVN 1 then put one drop of Dorzolamide-Timolol (a medication used to treat glaucoma, a condition in which the pressure inside the eye is abnormally high) in Resident 10's right eye. Then LVN 1 took off the gloves and left Resident 10's room. LVN 1 did not perform hand hygiene after taking off the gloves. During an interview on 10/17/23 at 1:21 p.m., LVN 1 stated, she had not performed hand hygiene after taking off the gloves. During an interview on 10/19/23 at 12:15 p.m., with the Director of Staff Development (DSD), DSD stated, LVN 1 was required to perform hand hygiene after LVN 1 removed the gloves she wore when she gave Resident 10 an eye drop. DSD stated, the failure to perform hand hygiene put Resident 10 at an increased risk of infection and the spread of infection. During a record review of Resident 10's Order Summary Report (ORD), dated 10/19/23, the ORD indicated, Dorzolamide HCL-Timolol Mal Ophthalmic Solution 22.3-6.8 mg/ml (Dorzolamide HCL-Timolol Maleate) Instill 1 drop in right eye three times a day for Glaucoma. During a review of Resident 10's Medication Administration Record (MAR), dated 10/1/23-10/31/23, the MAR indicated, LVN 1 gave one drop of Dorzolamide HCL-Timolol Mal in Resident 10's right eye on 10/17/23 at 2:00 p.m. During a review of the facility's policy and procedure (P&P) titled, Handwashing/Hand Hygiene, undated, the P&P indicated, 8. Hand hygiene is the final step after removing and disposing of personal protective equipment. When removing gloves . Hold the removed glove in the gloved hand and remove the other glove . Perform hand hygiene.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to administer medications below a five percent (5%) error...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to administer medications below a five percent (5%) error rate when: 1. Licensed Vocational Nurse (LVN )1 gave Insulin Aspart (a drug used to treat diabetes; a condition that develops when a person's blood sugar is too high) 2 units, late to one (Resident 10) of 10 sampled residents. 2. LVN 1 gave Metformin 850 mg (a drug used to treat diabetes; a condition that develops when a person's blood sugar is too high), after lunch was finished and not with lunch, to one (Resident 12) of 10 sampled residents. These errors resulted in Resident 10 and 12, not receiving medication as prescribed by their physicians. Findings: During a review of Resident 10's admission Record (AR), dated 10/19/23, the AR indicated Resident 10 was originally admitted to the facility on [DATE], and had a diagnosis of Diabetes Mellitus (a condition that develops when a person's blood sugar is too high). During a review of Resident 12's admission Record (AR), dated 10/19/23, the AR indicated Resident 12 was originally admitted to the facility on [DATE], and had a diagnosis of Diabetes Mellitus. During a concurrent observation and interview on 10/17/23 at 1:08 p.m., with LVN 1, LVN 1 was observed giving the medication, Metformin 850 mg, to Resident 12. LVN 1 stated, Metformin was ordered to be given with lunch. Resident 12's lunch tray had already been removed and the tray cart taken back to the kitchen, when LVN 1 gave Metformin to Resident 12. LVN 1 stated, she gave Metformin after Resident 12 had eaten. During a concurrent interview and record review on 10/17/23 at 1:11 p.m., with LVN 1, Resident 12's medication administration record (MAR) was reviewed. The MAR indicated, metFORMIN HCL Oral Tablet 850 MG (Metformin HCL) Give 1 tablet by mouth with meals for DM (DM - Diabetes Mellitus). LVN 1 stated, she gave the Metformin, after Resident 12 had eaten. During an observation on 10/17/23 at 2:12 p.m., LVN 1 was observed giving the medication, Insulin Aspart 2 units, to Resident 10. During a concurrent interview and record review on 10/17/23 at 2:15 p.m., with LVN 1, Resident 10's MAR was reviewed. The MAR indicated, Insulin Aspart Injection Solution . inject as per sliding scale if 70 - 150 = No insulin . 151-200 = 2 units 201 - 250 = 3 units, 251 - 300 = 4 units . before meals and at bedtime for DM. LVN 1 stated, she checked Resident 10's blood sugar at 11:00 a.m. LVN 1 stated, the blood sugar was 166, and per the sliding scale she needed to give 2 units to Resident 10. LVN 1 stated, Resident 10 ate his lunch around noon. She stated, she usually gave Resident 10 his insulin between 11:00 a.m. and 11:30 a.m. LVN 1 stated, she gave the insulin after lunch because Resident 10 was in the physical therapy room before lunch and she couldn't give the medication to him there. LVN 1 stated, she had not checked the blood sugar again after 11:00 a.m. During a review of Resident 12's Order Summary Report (ORD), dated 10/19/23, the ORD indicated, Resident 12 was ordered metFORMIN HCL Oral Tablet 850 MG (Metformin HCL) Give 1 tablet by mouth with meals for DM. During a review of Resident 10's Order Summary Report (ORD), dated 10/19/23, ORD indicated, Resident 10 was ordered Insulin Aspart Injection Solution . inject as per sliding scale if 70 - 150 = No insulin . 151-200 = 2 units 201 - 250 = 3 units, 251 - 300 = 4 units . before meals and at bedtime for DM. During a review of Resident 10's Insulin Aspart Injection Solution 100 UNIT/ML (Insulin Aspart) Administration History (ADH), dated 10/19/23, the ADH indicated, Resident 10 was given 2 Units of Insulin Aspart by LVN 1 on 10/17/23 at 2:12p.m. During an interview on 10/18/23 at 3:35 PM with Director of Nursing (DON), DON stated, Resident 12 should have been given Metformin while she was eating lunch, not after she had eaten and the tray removed, as Metformin was ordered to be given with meals. DON stated, giving Metformin after lunch was an error and could have negatively affected the resident's blood sugar and health. DON stated, Resident 10's Insulin Aspart should have been given before lunch, as it was ordered to be given before lunch. DON stated, giving the Insulin Aspart after lunch was an error and could have negatively affected the resident's blood sugar and health. During a review of the facility's policy and procedure titled, Administering Medication, undated, indicated . 3. Medications must be administered in accordance with the orders, including any required time frame.
CONCERN (F)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected most or all residents

Based on observation, interview, and record review, the facility failed to store food safely when food in the refrigerator, chest freezer, reach-in freezer, and dry storage were unlabeled and undated....

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Based on observation, interview, and record review, the facility failed to store food safely when food in the refrigerator, chest freezer, reach-in freezer, and dry storage were unlabeled and undated. This failure has the potential of placing 21 out of 21 residents at risk for foodborne illnesses. Findings: During a concurrent observation and interview on 10/16/23, at 9:38 a.m., with Kitchen Supervisor (KS), during initial kitchen tour, in the chest freezer, 5 bags of broccoli had no date, two Ziploc bags of corn on the cob did not have label or date, and one package of turkey sausage with a date of 6/17/23. In the reach-in freezer, two bags totaling 24 veggie patties were without date and appeared with ice crystals inside the bag, two clear bags totaling 12 cheese pizzas were without label or date, 1 bag of frozen turkey was dated 6/23/23, 5 brown bags of French fries were unlabeled and undated, one package of frozen chopped meat was unlabeled and undated, and three bags of frozen raw chicken was unlabeled and undated. Inside the dry storage area, four 1-gallon containers of mayonnaise were not dated, two 5-lb bottles of Teriyaki Baste & Glaze dated 8-13-22. In the reach in-refrigerator, one 1-gallon jar of mayonnaise was without open date. KS stated canned goods are usually good for 6 months from the receive-by date then gets thrown away. KS also stated, it is important to have open dates and receive by dates because staff need to know when items need to be used. During an interview on 10/18/23 at 9:30 a.m., with Registered Dietician (RD), RD stated, all food items need to have dates. Her expectation is for the kitchen to be well organized and all food items labeled with dates. RD stated, it is important to have dates because food items can be kept a long time and staff need to know when to use them. During a review of the facility's policy and procedure titled Labeling and Dating of Foods, dated 2023, indicated All food items in the storeroom, refrigerator, and freezer need to be labeled and dated.
MINOR (B)

Minor Issue - procedural, no safety impact

Safe Environment (Tag F0921)

Minor procedural issue · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 80 square foot of space per resident for resid...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 80 square foot of space per resident for residents who occupied 3 multi-bed bedrooms. This condition had the potential to result in lack of sufficient space for the provision of care both routine and emergency and for residents to have their personal belongings at bedside. Findings: During multiple room observations on 10/16/23 through 10/19/23, there were three residents in Rooms 3, 5 and 10, which are 4 bed rooms. 1. room [ROOM NUMBER] measured 20.4 feet by 14 feet which equaled 71.4 square feet per resident. 2. room [ROOM NUMBER] measured 20.4 feet by 14 feet which equaled 71.4 square feet per resident. 3. room [ROOM NUMBER] measured 20.4 feet by 14 feet which equaled 71.4 square feet per resident. During random observations of care and services from 10/16/23 to 10/19/23, there was sufficient space for the provision of care for the residents in all rooms. There were no heavy equipment in the rooms that might interfere with residents care and each resident had adequate personal space and privacy. There were no complaints from residents regarding insufficient space for their belongings. During an interview on 10/19/23, at 9:58 a.m., with Resident 178, Resident 178 stated, he had sufficient space in his room. Resident 178 stated, he liked his room. During an interview on 10/19/23, at 10:31 a.m., Resident 178, Resident 178 stated, he liked his room and had room for his personal belongings. There were no negative consequences from decreased space. No safety concerns for residents in the three rooms. Granting of room size waiver recommended.
Apr 2022 7 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to meet the needs for two (Resident 8 and Resident 10) of 16 sampled r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to meet the needs for two (Resident 8 and Resident 10) of 16 sampled residents when the facility did not develop and implement a care plan for Resident 8's dialysis (treatment of kidney failure that rids your blood of unwanted toxins, waste products and excess fluids by filtering your blood) care and for Resident 10's hospice care. This deficient practice may result in Resident 8 and Resident 10's physical, psychosocial and functional needs to go unmet. Findings: 1. A review of Resident 8's Facesheet, dated 4/20/22, the face sheet indicated Resident 8 was admitted on [DATE] with a diagnosis of an infected dialysis catheter (tube inserted into the vein). A review of Resident 8's Minimum Data Set (MDS- an assessment tool) dated 2/10/22, the MDS indicated Resident 8 is on dialysis treatment. During an interview on 4/20/22 at 9:53 a.m. with Dialysis Nurse, Dialysis Nurse stated, Resident 8 had been receiving dialysis at Dialysis Nurse's clinic since February 2022. Dialysis Nurse stated, the dialysis access site for Resident 8 had been her left upper chest catheter. Dialysis Nurse further stated, Resident 8's left upper arm graft had not been used since admission in February 2022. During a concurrent record review of Resident 8's care plan on 4/21/22 at 11:16 a.m. with Director of Nursing (DON), DON stated, the care plan for Resident 8 was not updated with the use of a dialysis catheter. She further stated, it is important to update the care plan because the care for a dialysis catheter is different from the care for a dialysis graft. 2. A review of Resident 10's Facesheet, dated 4/21/22, Facesheet indicated, Resident 10 was admitted on [DATE], under palliative care (specialized care that focuses on providing patients relief from pain and other symptoms of a serious illness, no matter the diagnosis or stage of disease). A review of Resident 10's MDS dated [DATE], MDS indicated, Resident 8 is on hospice (end of life care). During a concurrent record review of Resident 10's care plan on 4/21/22 at 11:27 a.m. with DON, there was no care plan for hospice care. DON stated, the hospice team does the care plan and any documents that are needed, the facility staff will ask from the hospice team. DON further stated, it is important for Resident 10's care plan to include hospice care to identify the services that are needed to better care for Resident 10. A review of the facility's policy (P&P) titled, Care Plans, Comprehensive Person-Centered, undated, the P&P indicated, 12. The comprehensive, person-centered care plan is developed within seven (7) days of the required comprehensive assessment (MDS). 13. Assessments of residents are ongoing and care plans are revised as information about the residents and the residents' conditions change. 14. The interdisciplinary Team must review and update the care plan: a. When there has been a significant change in the resident's condition;
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0698 (Tag F0698)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview record review, the facility failed to provide care for one (Resident 8) requring dialysis when staff did not ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview record review, the facility failed to provide care for one (Resident 8) requring dialysis when staff did not do a complete physical assessment before and after Resident 8's dialysis treatment. This deficient practice resulted in an incomplete assessment of Resident 8's dialysis access site before treatment. Findings: A review of Resident 8's admission Record, the admission Record indicated, Resident 8 was admitted on [DATE], with a diagnosis of infected dialysis catheter. A review of Resident 8's Minimum Data Set (MDS- an assessment tool) dated 2/10/22, the MDS indicated, Resident 8 is on dialysis. During an interview on 4/20/22, at 9:53 a.m. with Dialysis Nurse, Dialysis Nurse stated, Resident 8 had been receiving dialysis at Dialysis Nurse's clinic since February 2022. Dialysis Nurse stated, the dialysis access site used for Resident 8 had always been the left upper chest catheter. Dialysis Nurse further stated, Resident 8's left upper arm graft had not been used since admission at the dialysis clinic in February 2022. During a concurrent record review of Resident 8's Hemodialysis Communication Notes, on 4/20/22, at 1:11 p.m. with Director of Nursing (DON), the Communication Notes for Resident 8 did not indicate vital signs and vascular access site were assessed before and after treatments in the month of April 2022. DON stated, Resident 8's vital signs and vascular site should be assessed before and after treatment to document any change that could happen before and after treatment.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to store medications according to manufacturer recommendations and label medications appropriately when one bottle of Dorzolamid...

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Based on observation, interview, and record review, the facility failed to store medications according to manufacturer recommendations and label medications appropriately when one bottle of Dorzolamide (prescription eye drops given for glaucoma, a condition where there is increased pressure in the eye) was stored in the refrigerator at 39 degrees Fahrenheit. This failure had the potential to cause resident to be administered ineffective medication resulting in worsening of their condition leading to damage of the eye. Findings: During a concurrent observation and interview on 04/20/2022, at 11:45 a.m., with Licensed Vocational Nurse 1 (LVN 1) inside the medication storage room, a bottle of dorzolamide was found stored inside the refrigerator. LVN 1 confirmed refrigerator temperature was 39 degrees Fahrenheit. LVN 1 stated, medications that are stored improperly could potentially be ineffective. During an interview with Director of Nursing (DON) on 04/20/2022 at 2:12 p.m., DON stated, medications should be stored according to manufacturer's recommendation. During a review of the medication insert for Dorzolamide given by the manufacturer, the insert indicated, the suggested storing conditions is between 59 and 86 degrees Fahrenheit. During a review of facility's policy and procedures titled Medication Storage in the Facility (undated), the policy stated Medications and biologicals are stored safely .properly, following manufacturer's recommendations .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure one nursing staff performed hand hygiene (handwashing or use of an alcohol-based hand sanitizer) during medication adm...

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Based on observation, interview, and record review, the facility failed to ensure one nursing staff performed hand hygiene (handwashing or use of an alcohol-based hand sanitizer) during medication administration when Licensed Vocational Nurse 1 (LVN 1) failed to perform hand hygiene after removing gloves after giving medications to Resident 5 and Resident 8. These failures had the potential to cause or spread infection which could result in hospitalization for Resident 5 and Resident 8. Findings: During an observation on 04/20/2022, at 9:00 a.m., outside of Resident 5's room, Licensed Vocational Nurse 1 (LVN 1), was observed doffing (taking off) gloves and exiting the resident's room after administering medications without performing hand hygiene. During a subsequent observation at 10:45 a.m., outside of Resident 8's room, LVN 1 also did not perform hand hygiene after doffing gloves after administering medication to Resident 8. During an interview on 04/20/2022, with Licensed Vocational Nurse 1 (LVN 1) , at 11:08 a.m., LVN 1 stated, hand hygiene should be done before entering resident rooms, after leaving resident rooms, between glove changes, before medication preparation, and before and after touching residents. LVN 1 confirmed she did not perform hand hygiene after all aforementioned events. LVN 1 further stated, hand hygiene when not done, can lead to spread of infection. During an interview on 04/20/2022, with Director of Nursing (DON), at 3:05 p.m., DON stated, staff to perform hand hygiene when going into resident rooms, coming out of resident rooms, before and after giving resident care. During a review of facility's policy and procedure titled, Handwashing/Hand Hygiene (undated), the policy indicated, All personnel shall follow the handwashing/hand hygiene procedures to help prevent the spread of infections to other personnel, residents, and visitors .Use an alcohol-based hand rub containing at least 62% alcohol; or, alternatively soap (antimicrobial or non-antimicrobial) and water for the following situations: .Before preparing or handling medications .After removing gloves .The use of globes does not replace handwashing/hand hygiene. Integration of globe use along with routine hand hygiene is recognized as the best practice for preventing healthcare-associated infections.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Menu Adequacy (Tag F0803)

Could have caused harm · This affected multiple residents

Based on observation, record review and interview, the facility failed to follow the lunch menu set for 4/18/22 when cut up watermelon was served to residents instead of apple crisp. This deficient p...

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Based on observation, record review and interview, the facility failed to follow the lunch menu set for 4/18/22 when cut up watermelon was served to residents instead of apple crisp. This deficient practice resulted in Resident 20 feeling disappointed. Findings: During a concurrent observation and interview on 4/18/22, at 10:45 a.m. with Dietary Manager (DM), there was cut up watermelon in the refrigerator. DM stated, it was left over from the weekend and it is still OK to use today. She further stated, it will be served for lunch. During an observation and interview on 4/18/22, at 12:38 p.m., Resident 20 was eating her lunch in her room and was reading the menu. Resident 20 noticed on the menu that apple crisp was the desert for 4/18/22's lunch. Resident 20 stated, there was no apple crisp on her lunch tray, but instead it was cut up watermelon. Resident 20 stated, she was disappointed there was no apple crisp. Resident 20 further stated, staff did not notify her of any changes in the menu this morning. During an interview on 4/21/22, at 10:42 a.m. with Registered Dietician (RD), RD stated menu changes should be communicated to the residents so that they will be aware.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to store food in a sanitary manner when ground pork was thawing on top of strawberry gelatin inside the refrigerator. This defi...

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Based on observation, interview, and record review, the facility failed to store food in a sanitary manner when ground pork was thawing on top of strawberry gelatin inside the refrigerator. This deficient practice had the potential to cause food borne illness and affect all residents. The facility census was 17. Findings: During a concurrent observation and interview on 4/18/22, at 10:45 a.m. in the kitchen, ground pork was thawing in a shallow pan on top of strawberry gelatin in the refrigerator. DM stated, thawing meat should be at the very bottom of the refrigerator and not on top of anything to prevent food borne illnesses. During an interview on 4/21/22, at 10:42 a.m. with Registered Dietician (RD), RD stated, thawing of any meat should be done at the very bottom of a refrigerator and never on top of any food to prevent food borne illnesses. A review of the facility's policy titled, Policy: Thawing of Meats, dated 2018, the policy indicated, a. Use a drip pan under food being thawed so drippings do not contaminate other food. B. Thaw meat on the bottom shelf below prepared, ready-to-eat foods.
MINOR (B)

Minor Issue - procedural, no safety impact

Deficiency F0912 (Tag F0912)

Minor procedural issue · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 9 of 17 residents in the following multiple re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to provide 9 of 17 residents in the following multiple resident bedrooms 3, 10, 15 with at least 80 square feet per resident. This failure had the potential to result in a lack of sufficient space for the provision of care by facility staff and for the lack of sufficient space for residents to have personal belongings at the bedside. Findings: During an observation on 4/20/22, accompanied by the Maintenance Supervisor (MS), MS measured the following multiple resident rooms in feet (ft) and inches (in): 1) a. room [ROOM NUMBER]: b. 20.4' x 14' c. Total Square Feet: 286.6 d. #Residents 2: 3 e. Square Feet/resident 71.4' 2) a. room [ROOM NUMBER]: b.20.4' x 14' c. Total Square Feet: 286.6 d. # Residents: 3 e. Square Feet/resident 71.4' 3) a. room [ROOM NUMBER] b. 20.4' 14' c. Total Square Feet: 286.6 d. # Residents: 2 e. Square Feet/resident 71.4' During an interview on 4/21/22 at 12:57p.m. with Administrator (Admin), Admin stated, there have been no complaints regarding space for resident rooms 3, 10, or 15 from staff or residents. There were no negative consequences attributable to the decreased space in rooms [ROOM NUMBER].
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • Grade B+ (80/100). Above average facility, better than most options in California.
  • • No major safety red flags. No abuse findings, life-threatening violations, or SFF status.
  • • No fines on record. Clean compliance history, better than most California facilities.
  • • 44% turnover. Below California's 48% average. Good staff retention means consistent care.
Concerns
  • • 27 deficiencies on record. Higher than average. Multiple issues found across inspections.
Bottom line: Generally positive indicators. Standard due diligence and a personal visit recommended.

About This Facility

What is We Care Skilled Nursing Facility's CMS Rating?

CMS assigns WE CARE SKILLED NURSING FACILITY an overall rating of 5 out of 5 stars, which is considered much above average nationally. Within California, this rating places the facility higher than 99% of the state's 100 nursing homes. This rating reflects solid performance across the metrics CMS uses to evaluate nursing home quality.

How is We Care Skilled Nursing Facility Staffed?

CMS rates WE CARE SKILLED NURSING FACILITY's staffing level at 3 out of 5 stars, which is average compared to other nursing homes. Staff turnover is 44%, compared to the California average of 46%. This relatively stable workforce can support continuity of care. RN turnover specifically is 83%, which is notably high. RNs provide skilled clinical oversight, so turnover in this role can affect medical care quality.

What Have Inspectors Found at We Care Skilled Nursing Facility?

State health inspectors documented 27 deficiencies at WE CARE SKILLED NURSING FACILITY during 2022 to 2025. These included: 25 with potential for harm and 2 minor or isolated issues.

Who Owns and Operates We Care Skilled Nursing Facility?

WE CARE SKILLED NURSING FACILITY is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility operates independently rather than as part of a larger chain. With 28 certified beds and approximately 24 residents (about 86% occupancy), it is a smaller facility located in HAYWARD, California.

How Does We Care Skilled Nursing Facility Compare to Other California Nursing Homes?

Compared to the 100 nursing homes in California, WE CARE SKILLED NURSING FACILITY's overall rating (5 stars) is above the state average of 3.2, staff turnover (44%) is near the state average of 46%, and health inspection rating (4 stars) is above the national benchmark.

What Should Families Ask When Visiting We Care Skilled Nursing Facility?

Based on this facility's data, families visiting should ask: "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" "Can I speak with family members of current residents about their experience?"

Is We Care Skilled Nursing Facility Safe?

Based on CMS inspection data, WE CARE SKILLED NURSING FACILITY has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 5-star overall rating and ranks #1 of 100 nursing homes in California. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at We Care Skilled Nursing Facility Stick Around?

WE CARE SKILLED NURSING FACILITY has a staff turnover rate of 44%, which is about average for California nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was We Care Skilled Nursing Facility Ever Fined?

WE CARE SKILLED NURSING FACILITY has no federal fines on record. CMS issues fines when nursing homes fail to meet care standards or don't correct problems found during inspections. The absence of fines suggests the facility has either maintained compliance or corrected any issues before penalties were assessed. This is a positive indicator, though families should still review recent inspection reports for the full picture.

Is We Care Skilled Nursing Facility on Any Federal Watch List?

WE CARE SKILLED NURSING FACILITY is not on any federal watch list. The most significant is the Special Focus Facility (SFF) program, which identifies the bottom 1% of nursing homes nationally based on persistent, serious quality problems. Not being on this list means the facility has avoided the pattern of deficiencies that triggers enhanced federal oversight. This is a positive indicator, though families should still review the facility's inspection history directly.