F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** THE
FOLLOWING DEFICIENCY REPRESENTS AN INCIDENT OF PAST NON-COMPLIANCE THAT WAS
SUBSEQUENTLY CORRECTED PRIOR TO THIS SURVEY. Based on record review, staff interview and
policy review, the facility failed to ensure medications were administered as ordered. This affected four (#50,
#11, #29 and #19) out of four residents reviewed for medication administration. The facility census was 49.
Findings include: 1. Review of Resident #50 closed medical record revealed an admission on [DATE] with
diagnoses including atrial fibrillation, heart failure, kidney failure and hypothyroidism. Review of Resident
#50 quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed intact cognition. Resident #50
required extensive assistance for bed mobility, transfers, and toileting. Review of the hospital discharge
record dated 03/31/25 Resident #50 was prescribed Levothyroxine 125 micrograms (mcg) one tablet by
mouth daily to start on 04/01/25. Review of the physicians' orders for Resident #50 for the month of March
2025 was silent for administration of levothyroxine. Review of the physicians' orders for Resident #50 for the
month of April 2025 was silent for administration of levothyroxine. Review of the medication administration
record (MAR) for Resident #50 was silent for any documentation of levothyroxine 125 mcg being
administered. Review of the progress notes for Resident #50 dated 04/30/25 at 09:44 P.M. revealed the
resident appeared to have blood in his stool and was not at baseline. The physician was notified, and
resident was transferred to the emergency room (ER). Review of the progress note for Resident #50 dated
05/01/25 revealed levothyroxine 125 mcg one tablet by mouth was omitted during order entry of hospital
discharge orders on 03/31/25 to begin on 04/01/25 and medication was not received. Resident #50 was
transferred to the ER due to low blood pressure and blood in his stool. Resident #50 was admitted with
hypothermia and hypothyroidism. Resident #50's physician and resident representative were notified.
Review of the facility medication error report for Resident #50 dated 05/01/25 revealed levothyroxine 125
mcg should have been initiated on 04/01/25 and was not. Immediate corrective action revealed that new
admission discharge orders will be brought to the morning meeting daily to ensure medication orders were
entered into the electronic medical record correctly. In addition, the facility conducted a whole facility audit
for all residents with thyroid diagnoses was conducted with emphasis on thyroid laboratory results being
current and medication correctly being administered. This included seventeen residents in the facility.
Interview on 07/02/25 at 12:00 P.M. with Director of Nursing (DON) verified the levothyroxine was not
entered into the computer on readmission on [DATE] and should have been. DON stated a medication error
report was completed on 05/01/25 and the family was notified of the error. 2. Review of current Resident
#11's medical record revealed an admission on [DATE] with diagnoses including vascular dementia, atrial
fibrillation, and myocardial infarction. Review of the quarterly MDS assessment dated [DATE] for Resident
#11 revealed an impaired cognition. Resident #11 required extensive assistance for toileting, bed mobility
and transfers. Resident #11 was coded as supervision for eating. Resident #11 was coded
(continued on next page)
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 3
Event ID:
365505
Printed: 05/15/2026
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
365505
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/02/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Village Green Rehabilitation and Healthcare Center
1315 Kitchen Aid Way
Greenville, OH 45331
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
as receiving an anticoagulant during the assessment period. Review of the plan of care for Resident #11
dated 03/26/25 revealed resident is at risk for abnormal bleeding or hemorrhage related to anticoagulant
therapy. Interventions include administering medications as prescribed, avoid activities that could cause
injury, monitor for signs and symptoms of bleeding, obtain and monitor laboratory results, and review
medications for adverse interactions. Review of the active physician orders for Resident #11 revealed an
order for Xarelto 20 milligrams (mg) one tablet daily for left atrial thrombus dated 03/24/25. Review of the
MAR for the month of March 2025 for Resident #11 revealed resident received Xarelto as ordered
beginning on 03/24/25. Review of the Medication Error Report dated 03/24/25 for Resident #11 revealed
Xarelto 20 mg was not entered into the electronic medical record during the transition to the new software
effective on 03/01/25. Immediate corrective actions included notification of the physician to restart orders
and obtain an echocardiogram. Further review of the medication error report revealed the resident
representative was notified. Interview on 07/02/25 at 12:00 P.M. with DON verified the medication error
occurred and the physician and Resident #11's representative was notified. DON verified the
echocardiogram was completed without any negative findings. 3. Review of current Resident #19 revealed
an admission date of 03/28/25 with diagnoses including chronic obstructive pulmonary disease, dementia,
kidney disease, and type two diabetes with polyneuropathy. Review of the comprehensive MDS
assessment dated [DATE] for Resident #19 revealed an intact cognition. Resident #19 required set up
assistance for meals, supervision for bed mobility and transfers and moderate assistance for toileting.
Review of the plan of care for Resident #19 dated 04/15/25 revealed resident has actual and potential for
pain related to arthritis, disc disease, obesity and type two diabetes with polyneuropathy. Interventions
include administering medications as ordered, encourage the resident to request pain medication as
needed, monitoring changes in mood and usual activities and effectiveness of pain medication. Review of
the active physicians orders for Resident #19 revealed an order dated 04/05/25 for
hydrocodone-acetaminophen tablet 5-325 mg give one tablet three times a day and pregabalin 50 mg one
tablet two times a day for pain. Review of the MAR for the month of April 2025 for Resident #19 revealed
hydrocodone-acetaminophen tablet 5-325 mg give one tablet three times a day and pregabalin 50 mg one
tablet two times a day for pain were signed off by nursing staff as administered on 04/19/25 at 6:00 P.M.
Further review of the individual patient-controlled substance administration record for Resident #19's
pregabalin and hydrocodone-acetaminophen revealed they were not signed out as administered on
04/19/25. Review of the medication error report dated 04/28/25 for Resident #19 revealed on 04/19/25 at
6:00 P.M. the resident did not receive the pregabalin and hydrocodone-acetaminophen as ordered. Further
review of the report revealed the Nurse Practitioner (NP) and the residents' power of attorney were notified
of the error on 04/21/25. Interview on 07/02/25 at 12:00 P.M. with the DON verified Resident #19 did not
receive prescribed medication (pregabalin and hydrocodone-acetaminophen) as ordered on 04/19/25 at
6:00 P.M. 4. Review of current Resident #29 medical record revealed an admission date of 04/01/24 with
diagnoses including anoxic brain damage, hypertensive heart disease, heart failure and peripheral
autonomic neuropathy. Review of the quarterly MDS assessment dated [DATE] for Resident #29 revealed
an intact cognition. Resident #29 was coded as dependent for eating and toileting assistance. Resident #29
required maximum assistance with bed mobility and transfers. Resident was coded as having pain during
the assessment period. Review of the plan of care for Resident #29 dated 04/21/25 revealed resident has
potential for pain related to inconsistent bowel pattern, contractures, head trauma, headaches, immobility,
and verbal complaints of pain. Interventions include administer medication as ordered, encourage the
resident to request pain medication as needed, monitoring changes in mood and usual activities and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365505
If continuation sheet
Page 2 of 3
Printed: 05/15/2026
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
365505
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/02/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Village Green Rehabilitation and Healthcare Center
1315 Kitchen Aid Way
Greenville, OH 45331
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
effectiveness of pain medication. Review of the active physician orders for Resident #29 revealed an order
for Pregabalin give 25 mg by mouth three times a day related to idiopathic peripheral autonomic neuropathy
dated 02/18/2025. Review of the MAR for Resident #19 for the month of April 2025 revealed the Pregabalin
was signed as administered on 04/19/25 at 6:00 P.M., by the nurse. Review of the medication error report
dated 04/28/25 for Resident #29 revealed the medication Pregabalin give 25 mg tabled was not
administered as ordered. Interview with resident denied any complaints of pain related to the incident.
Further review of the document revealed the physician and the resident representative were notified.
Interview on 07/02/25 at 12:00 P.M. with DON verified Resident #29's Pregabalin was not signed off on the
individual patient-controlled substance administration record indicating it was not administered on 04/28/25.
DON stated with the recent sale of the facility and the move to the new electronic health record the
controlled substance record was unable to be located at the time of the survey. Review of the facility policy
titled Medication Errors dated 09/2021, stated the medication error report should be completed in the
electronic health record with each error. Medication errors are to be reported to the physician and the
director of nursing. The deficient practice was corrected on 05/18/25 when the facility implemented the
following corrective actions: Review of the Episodic Event/Past Non-Compliance document revealed the
date of the event was 03/01/25. The form was documented as completed on 05/18/25. Facility documented
medication errors occurred from transcription at the time of change over to the new medical record software
due to the sale of the facility. Nurses were manually inputting all orders into the new system when some of
the errors occurred. As a result of the errors all medication records of residents in the facility at the time of
the change of owners were audited. No further medication errors were noted. On 05/01/25 a medication
audit was completed for all residents receiving levothyroxine in the facility. All medication orders were
confirmed correct and laboratory results for thyroid levels were confirmed or ordered to ensure levels were
within normal limits. On 05/05/25 all new admissions for the last 30 days will have medication and treatment
audits to ensure medications are entered into the electronic health record accurately. Fifteen resident
records were identified as new admissions. Each record was reviewed by two separate nurses and
documented on the new admission order check verification form. No further concerns were identified
regarding medication administration. On 05/13/25, audits for residents identified as receiving thyroid
medications were completed without any additional negative findings. On 05/18/25, audits for all new
admissions in the last thirty days were completed and no further concerns were identified regarding
medication administration. Review of the facility's new admission order check verification documentation
dated 05/07/25 through 06/24/25 revealed no new medication errors. By 05/18/25, the DON or designee
completed in-service training with all nurses regarding medication administration policies and procedures.
This deficiency represents non-compliance investigated under the Complaint Number OH00165552
(1377615).
Event ID:
Facility ID:
365505
If continuation sheet
Page 3 of 3