F 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, record review, interview and facility policy review the facility failed to maintain a medication
error rate of five percent or less. This affected one resident (#45) of six residents observed during
medication administration. The facility census was 86.Findings include: 1. On 11/26/25 at 9:00 A.M. through
11:16 A.M. and 12/01/25 from 8:08 A.M. through 8:21 A.M. medication pass was observed for six residents
(#2, #30, #45, #73, #75, and #76) provided by five facility staff nurses. A total of 26 observations were
made with two errors resulting in an error rate of 7.69%.Record review of Resident #45's medical record
revealed an admission date of 04/02/2019. Diagnoses include unspecified dementia without behavioral
disturbance, psychotic disturbance, mood disturbance and anxiety, chronic kidney disease stage III,
unspecified atrial fibrillation, other specified peripheral vascular diseases, essential (primary) hypertension,
anemia, presence of cardiac pacemaker, dysphagia oropharyngeal phase, muscle weakness, edema,
vitamin deficiency, nail dystrophy, presence of intraocular lens, and long term (current) use of
anticoagulants.Review of Resident #45's Minimum Data Set (MDS) dated [DATE] revealed a Brief Interview
for Mental Status (BIMS) could not be completed due to resident is rarely/never understood and confirms
Resident #45's cognitive skills for daily decision making is severely impaired.Review of Resident #45's
Medication Administration Record (MAR) dated 12/01/25 revealed Resident #45 had an order for
Metoprolol Succinate Oral Capsule ER 24 Hour Sprinkle 100 milligrams (mg) instructions include give one
capsule by mouth one time a day for hypertension and hold if systolic blood pressure is less than 110 with
an order date of 12/23/24. Resident #45 had an order for Potassium (electrolyte) tablet instructions include
give 20 milliequivalent (mEq) by mouth one time a day for hypokalemia with an order date of
12/22/19.Observation on 12/01/25 at 8:25 A.M. of Licensed Practical Nurse (LPN) #74 during medication
administration revealed Resident #45 receive Metoprolol Succinate ER 100 mg, one tablet, Potassium CL
ER 20 mEq, one tablet, and Eliquis (anticoagulant) 2.5 mg, one tablet. The three medication tablets were
then crushed and placed in pudding and administered to Resident #45. Observation of medication cards for
Metoprolol Succinate ER 100mg and Potassium CL ER 20 mEq were labeled do not crush on left upper
corner.Interview 12/01/25 at 9:10 A.M. with LPN #74 confirmed the medications provided were crushed and
administered to Resident #45.LPN #47 was observed to call Pharmacist #20 on speaker phone on
12/01/25 at 9:14 A.M. and Pharmacist #20 confirmed Metoprolol Succinate ER 100 mg tablet and
Potassium CL ER 20 mEq tablet should not be crushed. Review of the facility's Administration of
Medications policy dated 09/09/25 confirmed staff who are responsible for medication will adhere to the 10
rights of medications administration. Right drug, compare the order with the medication administration
record (eMAR) for accuracy and compare the label on the drug to the information on the eMAR, three
times. Verify the right resident. Right dose and if there is any doubt about the dose on the MAR or if there is
a question on the drug, stop and verify all information before administering. Review of the facility's policy
titled, Medication - Related Errors dated 05/01/10 confirms if a
Residents Affected - Few
(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 4
Event ID:
365410
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
365410
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/01/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mayfair Village Nursing Care C
3000 Bethel Rd
Columbus, OH 43230
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 0759
Level of Harm - Minimal harm
or potential for actual harm
medication reaches a resident in error, the facility should, notify the pharmacy of ay possible dispensing
occurrence; and notify physician/prescriber and obtain further instructions and/or orders. Facility staff
should monitor the resident in accordance with physician/prescriber's instructions.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365410
If continuation sheet
Page 2 of 4
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
365410
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/01/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mayfair Village Nursing Care C
3000 Bethel Rd
Columbus, OH 43230
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 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, record review, and facility policy review the facility failed to administer medications as ordered
for Resident #45. This affected one of five residents observed during medication administration. The facility
census was 86.Findings include:Record review of Resident #45's medical record revealed an admission
date of 04/02/2019. Diagnoses include unspecified dementia without behavioral disturbance, psychotic
disturbance, mood disturbance and anxiety, chronic kidney disease stage III, unspecified atrial fibrillation,
other specified peripheral vascular diseases, essential (primary) hypertension, anemia, presence of cardiac
pacemaker, dysphagia oropharyngeal phase, muscle weakness, edema, vitamin deficiency, nail dystrophy,
presence of intraocular lens, and long term (current) use of anticoagulants.Review of Resident #45's
Minimum Data Set (MDS) dated [DATE] revealed a Brief Interview for Mental Status (BIMS) could not be
completed due to resident is rarely/never understood and confirms Resident #45's cognitive skills for daily
decision making is severely impaired.Review of Resident #45's Medication Administration Record (MAR)
dated 12/01/25 revealed Resident #45 had an order for Metoprolol Succinate Oral Capsule ER
(antihypertensive) 24 Hour Sprinkle 100 MG instructions include give one capsule by mouth one time a day
for hypertension and hold if systolic blood pressure is less than 110 with an order date of 12/23/24.
Resident #45's Potassium (supplement) tablet instructions include give 20 mEq by mouth one time a day
for hypokalemia with an order date of 12/22/19.Observation on 12/01/25 at 8:25 A.M. of License Practical
Nurse (LPN) #74 during medication administration revealed Resident #45 receive Metoprolol Succinate ER
100mg one tablet, Potassium CL ER 20 mEq one tablet, and Eliquis 2.5 mg one tab. The three medication
tablets were then crushed and placed in pudding and administered to Resident #45. Observation of
medication cards for Metoprolol Succinate ER 100mg one tablet and Potassium CL ER 20 mEq one tablet
were labeled do not crush on left upper corner.Interview 12/01/25 at 9:10 A.M. with LPN #74 confirmed the
three medications were crushed and administered to Resident #45.Observation on 12/01/25 at 9:14 A.M. of
LPN # 47's interview with Pharmacist #20 confirmed Metoprolol Succinate ER 100 mg tablet and
Potassium CL ER 20 mEq tablet should not be crushed.LPN #47 was observed to call Pharmacist #20 on
speaker phone on 12/01/25 at 9:14 A.M. and Pharmacist #20 confirmed Metoprolol Succinate ER 100 mg
tablet and Potassium CL ER 20 mEq tablet should not be crushed. Review of the facility's Administration of
Medications policy dated 09/09/25 confirmed staff who are responsible for medication will adhere to the 10
rights of medications administration. Right drug, compare the order with the medication administration
record (eMAR) for accuracy and compare the label on the drug to the information on the eMAR, three
times. Verify the right resident. Right dose and if there is any doubt about the dose on the MAR or if there is
a question on the drug, stop and verify all information before administering. Review of the facility's policy
titled, Medication - Related Errors dated 05/01/10 confirms if a medication reaches a resident in error, the
facility should, notify the pharmacy of any possible dispensing occurrence; and notify physician/prescriber
and obtain further instructions and/or orders. Facility staff should monitor the resident in accordance with
physician/prescriber's instructions.This violation represents non-compliance investigated under Complaint
Number 2647703.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365410
If continuation sheet
Page 3 of 4
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
365410
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
12/01/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mayfair Village Nursing Care C
3000 Bethel Rd
Columbus, OH 43230
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 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and facility policy review the facility failed to properly label and store medications.
This had the potential to affect all residents who receive medications from the facility. The census was
86.Findings include: 1. Observation on [DATE] at 9:39 A.M. with Licensed Practical Nurse (LPN) #52 during
medication administration revealed a facility stock bottle of Thiamine B1 (vitamin) 100 milligram (mg) tablet
which was opened and undated, a facility stock bottle of Famotidine (decreases acid in the stomach) 20 mg
bottle which was opened and undated, and container of MiraLAX (laxative)17 mg which was opened and
undated. Other facility stock medication bottles were observed in medication cart had open dates written on
top of lid of medication bottle.Interview on [DATE] at 9:45 A.M. with LPN #52 confirmed the bottles of
Thiamine, Famotidine, and MiraLAX were open but were not labeled with the open date. LPN #52 was
observed labeling the bottles. 2. Observation on [DATE] at 11:25 A.M. of the medication storage room
revealed unopened but expired items including a bottle of Fiber Powder Psyllium husk with the expiration of
[DATE], a bottle of Vitamin A 3,000 mcg, B2 Riboflavin with an expiration date of [DATE], nasal spray
moisturizing spray with an expiration date of [DATE], and nasal decongestant PE Phenylephrine HCL 10
mg expiration date of [DATE].Interview on [DATE] at 11:45 A.M. with the Assistant Director of Nursing
(ADON) confirmed the medications were expired.Review of the facility's policy titled, Storage and Expiration
Dating of Medications and Biologicals last revised on [DATE] confirms the facility should ensure
medications and biologicals that: (1) have an expired date on the label; (2) have been retained longer than
recommended by manufacturer or supplier guidelines,: or (3) have been contaminated or deteriorated, are
stored separate from other medications until destroyed or returned to the pharmacy or supplier.
Event ID:
Facility ID:
365410
If continuation sheet
Page 4 of 4