Celebrate Senior Living Of Fort Wayne
Inspection Findings
F-Tag F0580
F 0580 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few
FORM CMS-2567 (02/99) Previous Versions Obsolete
10/14/25 as ordered. Resident T took 1 dose of Losartan on 10/20/25 but refused the medication all other days of the month. She refused Spironolactone every day in the month of October.A MAR, dated November 2025, indicated the resident had not taken any oral medications, including Losartan and Spironolactone, from 11/1 through 11/17/25.There was no documentation completed, indicating the physician or NP had been notified of the residents refusal of oral medications, including refusals of Losartan and Spironolactone, in September, October, or November 2025. The NP treated Resident T's acute kidney injury in October 2025 by holding her doses of Losartan and Spironolactone from 10/10-10/14/25, however,
the resident hadn't been taking the medications prior to or after the medications were held.On 11/18/25 at 12:44 P.M., the NP was interviewed. He indicated he was aware of Resident T's occasional refusal of medications but had not known the resident was not taking her medications routinely as ordered. He indicated he ordered her Losartan and Spironolactone held for 5 days, 10/10-10/14/25, to see if the medications had contributed to the rise in her blood creatinine. He had not been aware the resident had refused these medications months prior to or after the medications were ordered to be held.In a confidential interview, staff member 2 indicated ordering providers were to be notified of resident's refusal to take prescribed medication.During a confidential interview, staff member 3 indicated when a resident refused a medication, the MAR would be marked with a 2 meaning refusal and a note documented in the nurse progress notes. The NP or doctor would be notified and documented in the nurse progress notes. A current facility policy, titled Change in a Resident's Condition or Status, was provided by the Director of Nursing on 11/18/25 at 2:24 P.M. The policy indicated staff would promptly notify the attending physician of changes in
the resident's medical/mental condition and/or status. The nurse was to notify the resident's physician when there had been a refusal of treatment or medications 2 or more consecutive times.This Citation relates to Intake 2646144.3.1-5(a)(3)
Event ID:
Facility ID:
If continuation sheet
Printed: 04/13/2026 Form Approved OMB No. 0938-0391
Department of Health & Human Services Centers for Medicare & Medicaid Services STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
B. Wing
A. Building
(X3) DATE SURVEY COMPLETED
11/19/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Celebrate Senior Living of Fort Wayne
3420 East State Blvd Fort Wayne, IN 46805
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency. (X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES (Each deficiency must be preceded by full regulatory or LSC identifying information)
F-Tag F0684
F 0684
Provide appropriate treatment and care according to orders, residentβs preferences and goals.
Level of Harm - Minimal harm or potential for actual harm
Based on interview and record review, the facility failed to ensure labs were completed as ordered by the physician for 1 of 3 residents reviewed (Resident T).Findings include:On 11/17/25 at 2:00 p.m., Resident T's
record was reviewed. Diagnoses included schizophrenia, heart failure, high blood pressure, and overactive bladder.Care plans indicated Resident T was prescribed anti-hypertensive and diuretic medications to treat high blood pressure. She was at risk for fluctuations in fluid balance and complications from bladder incontinence. Interventions included obtaining and monitoring lab/diagnostic work as ordered.A physician order, dated 10/10/25, was to collect a urinalysis (UA) for culture and sensitivity.A physician's progress note, dated 10/10/25, indicated Resident T had been seen by the Nurse Practitioner (NP) due to abnormal kidney function. The resident had lab work completed on 10/8/25. The lab results indicated blood creatinine level was elevated at 2.17. The resident did not have a history of chronic kidney disease, and her baseline creatinine was <1.0. When asked, the resident denied any urinary tract infection (UTI) related symptoms.
The plan included obtaining a urinalysis to check for possible causes of her elevated blood creatinine level.An article, titled Creatinine and Acute Kidney Injury (AKI) was retrieved from kidney.org on 11/17/25 at 3:25 P.M. The article indicated too much creatinine in the blood could be a sign of possible kidney problems. AKI was a sudden episode of kidney failure or damage within a short period of time. AKI causes
a build-up of waste products in the blood, affects other organs such as the brain, heart, and lungs. There are several causes of AKI including side effects of medications, direct damage to the kidney or blockage of
the urinary tract. Tests used to diagnose and investigate the cause of AKI include urinalysis (a urine test used to find signs of kidney disease and kidney failure).A nurse progress note, dated 10/16/25 at 4:02 p.m., indicated the UA results were in and no pathogens (disease causing organisms) were detected. The Nurse Practitioner (NP) was notified with no new orders given.A lab report, dated 10/16/25, was provided by the Director of Nursing (DON) on 11/18/25 at 12:32 P.M. The report indicated there were no organisms detected in Resident T's urine test. The DON indicated only a culture and sensitivity was done on the urine and not a urinalysis as ordered by the NP but should have been. The DON indicated the specialty lab where the urine test had been sent, detected only pathogens in the urine but didn't process urinalysis tests.On 11/18/25 at 12:44 P.M., the NP was interviewed. He indicated he had ordered a urinalysis with culture and sensitivity if indicated as follow-up to the residents abnormal blood creatinine level. When asked, he indicated, the facility used a special laboratory, able to detect pathogens in the urine as well as best medications to use in treating the organisms. He indicated his understanding from the laboratory, was urinalysis would be completed in addition to detection of pathogens. A facility policy, provided by the nurse manager on 11/19/25 at 10:14 A.M., indicated the facility would obtain laboratory services through licensed laboratories, upon the order from a facility medical provider. Nursing staff would initiate providers orders, ensure timely collection, and collect specimens as ordered per the nurse's scope of practice.This Citation relates to Intake 2646144.
Residents Affected - Few
FORM CMS-2567 (02/99) Previous Versions Obsolete
Event ID:
Facility ID:
If continuation sheet
CELEBRATE SENIOR LIVING OF FORT WAYNE in FORT WAYNE, IN inspection on recent inspection.
Found 0 violation(s). Severity: Standard violations. Status: 0 corrected, 0 pending.
Frequently Asked Questions
- What is an F-tag violation?
- F-tags are federal deficiency codes used by CMS to categorize nursing home violations. Each F-tag corresponds to a specific federal regulation (42 CFR Part 483). For example, F607 relates to abuse prevention policies, F880 relates to infection control.
- Were these violations corrected?
- Facilities must submit plans of correction and implement changes within required timeframes. CMS conducts follow-up inspections to verify corrections. Check the inspection report for specific correction dates and follow-up verification status.
- How often do nursing home inspections happen?
- CMS conducts unannounced inspections of all Medicare/Medicaid-certified nursing homes at least once per year. Additional inspections may occur based on complaints, facility-reported incidents, or follow-up to verify previous violations were corrected.
- What should families do about these violations?
- Families should: (1) Review the full inspection report for details, (2) Ask facility administration about specific corrective actions taken, (3) Check if this represents a pattern by reviewing prior inspections, (4) Compare with other facilities in FORT WAYNE, IN, (5) Report new concerns to state authorities.
- Where can I see the full inspection report?
- Complete inspection reports are available on Medicare.gov's Care Compare website (www.medicare.gov/care-compare). You can also request copies directly from CELEBRATE SENIOR LIVING OF FORT WAYNE or from the state Department of Health. Reports include deficiency codes, facility responses, and correction timelines.