F 0558
Reasonably accommodate the needs and preferences of each resident.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review the facility failed to ensure call lights were within reach at all times
for Residents #32, #5, and #25. This affected three of three residents reviewed for environmental concerns.
The facility census was 46.
Residents Affected - Few
Findings include:
1. Resident #32 was admitted to the facility on [DATE] with diagnoses of cerebellar stroke syndrome,
atherosclerotic heart disease, hypertension, difficulty walking, muscle weakness and cognitive
communication deficit. Her comprehensive assessment dated [DATE] revealed she was severely cognitively
impaired for decision making and had functional limitations of both hands.
Observation on 07/09/19 at 10:42 A.M. of Resident #32 revealed her push button type call light was not
within her reach. This was verified by State Tested Nursing Assistant (STNA #132) at the time of the
observation.
On 07/09/19 at 10:46 A.M. interview with Resident #32's daughter revealed she was concerned that her
mother could not reach the call light. The daughter said she was unsure if her mother could push the button
due to contracted fingers on both hands and thought a flat, touch-pad type of call light would be easier. This
was verified by STNA #132 who revealed she was unsure why Resident #32 was not provided with a
touch-pad type of call light.
2. Resident #5 was admitted to the facility on [DATE] with diagnoses of dementia, heart failure, morbid
obesity, hypertension, osteoarthritis, anxiety, shortness of breath, muscle weakness and psychosis. Her
comprehensive assessment dated [DATE] revealed she had functional limitations of both hands.
Observation on 07/09/19 at 10:51 A.M. of Resident #5 revealed her call light was not within her reach. This
was verified at 10:52 A.M. by STNA #162.
On 07/09/19 at 10:52 A.M. interview with STNA #162 revealed Resident #5 was not able to use the push
button type call light, but might be able to use a touch-pad call light. STNA #162 verified all residents' call
lights must be kept within reach at all times.
3. Resident #25 was admitted to the facility on [DATE] with diagnoses of Alzheimer's disease, and a history
of falling. His comprehensive assessment dated [DATE] revealed he required extensive assistance for bed
mobility and had limited range of motion.
(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:
365774
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
365774
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/12/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Bsd Opco LLC
550 Miner Dr
Medina, OH 44256
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 0558
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Observation on 07/09/19 at 11:01 A.M. of Resident #25 revealed his call light was not within reach. This
was verified by STNA #132 who stated he used his call light frequently.
On 07/12/19 at 2:11 P.M. interview with the Director of Nursing (DON) revealed touch-pad type call lights
were available. The DON verified all call lights must be kept in reach of the resident, and they should have
recognized the need for a more suitable call light (touch-pad) for Resident #5 and Resident #32.
Review of the call light policy dated November 2015 revealed all residents must have a working call light
and it must be in their reach at all times while in their room. Staff must remind the resident where it was and
show them how to use it.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365774
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
365774
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/12/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Bsd Opco LLC
550 Miner Dr
Medina, OH 44256
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
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 review of manufacturer's instructions the facility failed to maintain
a medication error rate of less than five percent. There were two errors out of 35 opportunities for a
medication administration error rate of 5.71 percent. This affected one (Resident #3) of three residents
observed for medication administration. The facility census was 46.
Residents Affected - Few
Finding include:
Resident #3 was admitted to the facility on [DATE] with diagnoses including hypertension and diabetes.
Review of the July 2019 physicians orders revealed an order for insulin according to a sliding scale (a dose
based on the resident's blood sugar level) to be given prior to meals and at bedtime. There was also an
order for Metoprolol 12.5 milligram (mg) to be given by mouth twice daily for high blood pressure. There
were no parameters or further instructions ordered pertaining to the Metoprolol.
Observation of medication administration on 07/10/19 at 8:15 A.M. for Resident #3 with Licensed Practical
Nurse (LPN) #133 revealed Resident #3 received insulin per a Novolog Flexpen (a device to administer
insulin). LPN #133 prepared the dose of insulin using the Novolog Flexpen without first priming the pen
(pressing the button on the device to remove air bubbles that may have collected in the cartridge) and gave
the injection of insulin in the resident's right upper forearm. LPN #133 took Resident #3's blood pressure
and did not administer the Metoprolol.
Review of the Medication Administration Record (MAR) time stamped 8:35 A.M. on 07/10/19 revealed the
Metoprolol 12.5 mg was signed off as administered.
Interview on 07/11/19 at 8:36 A.M. with LPN #133 revealed she did not give the resident's Metoprolol due to
a blood pressure of 107/48 and a heart rate of 66 beats per minute. LPN #133 verified she made a mistake
and signed off the Metoprolol as administered and stated the physician did not need to be notified unless
two doses were held. LPN #133 also verified she did not prime the Flexpen to expel air bubbles to ensure
an accurate dose of insulin was administered.
On 07/11/19 at 10:35 A.M. interview with the Director of Nursing (DON) revealed the facility's policy was to
hold blood pressure medication if the heart rate was under 60 beats per minute and to notify the physician if
blood pressure medication was not administered. The DON verified LPN #133 did not administer Resident
#3's insulin or Metoprolol as ordered which resulted in a medication error rate of 5.71 percent.
Review of the Novolog Flexpen manufacturer's instructions revealed to prime the cartridge to remove any
air bubbles prior to injection.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365774
If continuation sheet
Page 3 of 3