F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review, review of facility policy and interviews, the facility failed to ensure advanced directives were
readily available and followed during a medical emergency for Resident #66. This affected one resident
(Resident #66) of three residents reviewed for advance directives. The facility census was 64.
Findings included:
Review of the medical record revealed Resident #66 was admitted to the facility on [DATE]. Diagnoses
included heart failure, respiratory failure, atrial fibrillation, congestive heart failure, nonrheumatic aortic
stenosis, atherosclerotic heart disease, cardiomyopathy, hypertension, major depressive disorder, transient
ischemic attack, and thoracic aortic ectasia. Resident #66 expired in the facility on [DATE].
Review of the physician's orders revealed Resident #66 had an order for Do Not Resuscitate Comfort
Care-Arrest (DNRCC-A) dated [DATE].
Review of the DNR identification form revealed Resident #66 requested a code status of
Do-Not-Resuscitate Comfort Care Arrest (DNRCCA). It was signed by the resident. The physician signed
on [DATE].
Review of the admission Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed Resident #66
had intact cognition.
Review of the plan of care dated [DATE] revealed Resident #66 has a DNRCCA code status. Interventions
included to adhere to his desired code status, inform the residents physician if there was a code status
change, and review the code status quarterly or as needed.
Review of the progress notes revealed no documentation of him expiring. The last health status note was
dated [DATE] at 9:09 A.M. There was a psychiatric progress note dated [DATE].
Review of the facility document titled Code Blue Bedside Documentation, dated [DATE] at 10:30 A.M.,
revealed the housekeeper witnessed Resident #66 drop to the floor to the ground. The bedside nurse went
into assess due to he had an absence of vital signs. Cardiopulmonary resuscitation (CPR) was initiated,
oxygen was placed on the resident. A nursing assistant called 911. Resident #66 had a return of his pulse
then his pulse was lost and CPR was initiated, Emergency Medical Service (EMS) arrived and CPR
continued. They were unable to return his vitals and the time of death was called at 10:45 A.M.
(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 6
Event ID:
365667
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
365667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Center for Rehabilitation and Nursing
555 Springbrook 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 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Review of the EMS run report dated [DATE] revealed the EMS received the call at 10:33 A.M. and was on
scene at 10:41 A.M. The narrative stated they responded to a call to the skilled nursing facility for a resident
who was unresponsive but breathing. Upon arrival the staff greeted the EMS at the entrance and informed
the resident had been found unresponsive in the bathroom at 10:30 A.M. He was last seen normal at 10:00
A.M. The resident had stopped breathing briefly in the past five minutes, provoking staff to perform CPR.
The staff said they got him back. EMS inquired about the code status and staff stated he was a DNR
however it was not signed and opted to treat the residents as a full code unless a valid DNR was produced.
Upon arrival to the residents' room the resident was supine on the floor with a nursing assistant at the
resident's head assisting with a respiration with Bag-Valve-Mask (BVM). The resident had no detectable
chest rise and fall, no apical pulse or carotid pulse. Chest compressions were initiated with intermittent
ventilation provided by the nursing assistant. CPR continued for one to two minutes until the signed DNR
was found. CPR was discontinued and the resident remained pulseless and apneic.
On [DATE] at 9:00 A.M. an interview with Registered Nurse (RN) #300 revealed when she walked into the
room of Resident #66 Agency RN #301 had already been performing CPR on him. She stated RN #301
could not find his code status so she initialed CPR. She stated she started to assist with CPR. She stated
then another nurse called out they found the DNR form however it was not signed so they continued CPR
until the EMS arrived. She stated the EMS took over CPR. She stated then the other nurse who was at the
desk found the signed DNR so EMS stopped CPR. She verified at this time CPR should not have been
started on Resident #66 due to his DNR status.
On [DATE] at 10:45 AM an interview with Agency RN # 301 revealed she walked into the room of Resident
#66 and he was on the floor without a pulse. She stated she did not know his code status and did not go
look before she started CPR. She stated she yelled at the housekeeper who was in the room to go get help.
She stated RN #300 came in and took over CPR. She stated the squad was called and they continued CPR
until the squad arrived. She stated they took over doing CPR then someone came in and stated he had a
signed DNRCC-A so the EMS stopped. She stated they did get a faint pulse but then nothing again. She
stated she would have started CPR anyway until she found out his code status. She stated she was not just
going to let him lay there and not initiate CPR.
Review of facility policy titled Advance Directives, dated 12/16, revealed Advance Directives would be
respected in accordance with state law and facility policy. The information about whether or not the resident
had executed an Advance Directive would be displayed prominently in the medical record. The plan of care
would be consistent with the residents documented Advanced Directives.
This deficiency represents non-compliance investigated under Complaint Number OH00152130.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365667
If continuation sheet
Page 2 of 6
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
365667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Center for Rehabilitation and Nursing
555 Springbrook 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 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Immediately tell the resident, the resident's doctor, and a family member of situations (injury/decline/room,
etc.) that affect the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
review of the medical record and interview with staff the facility failed to notify the physician when Resident
#65 was not administered routine insulin according to the physician order. This affected one resident (
Resident #65) of three reviewed for insulin administration. The facility census was 64.
Findings included:
Review of the medical record revealed Resident #65 was admitted to the facility on [DATE]. Diagnoses
included fracture of the left humerus, cervical sprain, chronic obstructive pulmonary disease, hypertension,
chronic kidney disease, diabetes, absence of left breast, breast cancer, diverticulosis, dry eye syndrome,
major depressive disorder, spinal stenosis, chronic migraines, bilateral cataracts, osteoarthritis of both
knees, peripheral vascular disease, and protein calorie malnutrition. She was discharged on 03/15/24 with
hospice services.
Review of a physician order revealed Resident #65 had an order for 64 units of degludec insulin dated
02/14/24. She also had orders for the aspart insulin per sliding scale before each meal dated 02/14/24 and
20 units before each meal dated 02/15/24.
Review of the admission Minimum Data Set 3.0 assessment dated [DATE] revealed Resident #65 had
intact cognition. She received insulin.
Review of the pharmacy delivery invoices dated 02/24/24 revealed Resident #65 had received three
degludec flex pens.
Review of the February 2024 and March 2024 Medication Administration Records (MAR) revealed Resident
#65 did not receive her deglu[DATE] units on 03/02/24 at 7:00 A.M. and a code 9 was documented on the
MAR to indicate it was not given and to see nurses note. Blood glucose readings were being monitored
three times a day in February and March. Review of the blood glucose checks between 02/14/24 and
03/01/24 for Resident #65 revealed multiple blood glucose readings over 250 milligrams per deciliter
(mg/dl) even with all insulin being given according to the physician orders.
Review of the electronic Medication Administration Record (eMAR) medication administration note dated
03/02/24 at 7:53 A.M. revealed Resident #65 had not received her 64 units of degludec because the facility
was waiting for it to be delivered from the pharmacy.
Review of progress notes and eMar notes for March 2024 revealed no findings to indicate the physician had
been notified of Resident #65 not receiving the degludec insulin as ordered on 03/02/24.
On 03/25/24 at 2:30 P.M. an interview with the Director of Nursing verified on 03/02/24 the degludec insulin
was in the refrigerator however the agency nurse did not look in the refrigerator and pull it out to give it
Resident #65. The DON also verfied there was no documentation of the physician being notified Resident
#65 did not receive the 64 units of degludec insulin on 03/02/24 at 7:00 A.M.
This deficiency represents non-compliance investigated under Complaint Number OH00151789.
This deficiency is an example of continued noncompliance from the survey dated 02/12/24.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365667
If continuation sheet
Page 3 of 6
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
365667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Center for Rehabilitation and Nursing
555 Springbrook 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 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
record review and interview the facility did not ensure Resident #65 was administered insulin according to
physician orders. This affected one resident ( Resident #65) of three residents reviewed for insulin
administration. The facility census was 64.
Residents Affected - Few
Findings include:
Review of the medical record revealed Resident #65 was admitted to the facility on [DATE]. Diagnoses
included fracture of the left humerus, cervical sprain, chronic obstructive pulmonary disease, hypertension,
chronic kidney disease, diabetes, absence of left breast, breast cancer, diverticulosis, dry eye syndrome,
major depressive disorder, spinal stenosis, chronic migraines, bilateral cataracts, osteoarthritis of both
knees, peripheral vascular disease, and protein calorie malnutrition. She was discharged on 03/15/24 with
hospice services.
Review of the admission Minimum Data Set 3.0 assessment dated [DATE] revealed Resident #65 had
intact cognition. She received insulin.
Review of a physician order revealed Resident #65 had an order for 64 units of degludec insulin dated
02/14/24 and was discontinued on 03/03/24. On 03/04/24 a physician order was written for 70 units of
degludec insulin each morning. Additional insulin orders included aspart insulin per sliding scale before
each meal dated 02/14/23 and 20 units aspart insulin before each meal dated 02/15/24.
Review of the February 2024 Medication Administration Record (MAR) for Resident #65 revealed her blood
glucose readings were to be measured three times per day and the readings indicated multiple blood
glucose readings over 250 milligrams per deciliter (mg/dl) even with all insulin being given according to the
physician orders.
Review of the pharmacy delivery invoices dated 02/24/24 revealed Resident #65 had received three
degludec flex pens.
Review of the electronic Medication Administration Record (eMAR) medication administration note dated
03/02/24 at 7:53 A.M. revealed Resident #65 had not received her 64 units of degludec because the facility
was waiting for it to be delivered from the pharmacy.
Review of the March 2024 Medication Administration Record (MAR) revealed Resident #65 did not receive
her deglu[DATE] units on 03/02/24 at 7:00 A.M. Blood glucose reading on 03/02/24 at 4:30 P.M. was
234mg/dl, on 03/03/24 at 7:00 A.M. it was 205 mg/dl and at 11:30 A.M. it was 207 mg/dl. She received an
extra four units of aspart insulin per sliding scale all three times. On 03/06/24 there was no documentation
of a blood glucose check at 4:30 P.M. and no aspart insulin per sliding scale was administered.
Review of the progress note dated 03/03/24 dated 6:52 P.M. revealed Resident #65 had an abnormally high
(no exact number was indicated in the note) blood glucose reading. Her husband was aware and anxious.
The physician was made aware and ordered to increase the degludec insulin to 70 units.
On 03/25/24 at 2:30 P.M. an interview with the Director of Nursing (DON) revealed on 03/02/24 the
degludec insulin was in the refrigerator however they agency nurse did not look in the refrigerator
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365667
If continuation sheet
Page 4 of 6
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
365667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Center for Rehabilitation and Nursing
555 Springbrook 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 0760
Level of Harm - Minimal harm
or potential for actual harm
and pull it out to give it Resident #65. She stated she reached out to the pharmacy and they indicated she
was sent enough degludec on 02/24/24 to last until 03/04/24 so it was too soon to reorder on 03/02/24. The
DON verfied all insulins were not administered as ordered for Resident #65.
This deficiency represents non-compliance investigated under Complaint Number OH00151789.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365667
If continuation sheet
Page 5 of 6
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
365667
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/26/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Medina Center for Rehabilitation and Nursing
555 Springbrook 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 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Safeguard resident-identifiable information and/or maintain medical records on each resident that are in
accordance with accepted professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
review of the medical record and interview with staff the facility failed to document the death of Resident
#66 in the medical record. This affected one resident ( Resident #66) of three reviewed for complete
medical record. The facility census was 64.
Finding included:
Review of the medical record revealed Resident #66 was admitted to the facility on [DATE]. Diagnoses
included heart failure, respiratory failure, atrial fibrillation, congestive heart failure, nonrheumatic aortic
stenosis, atherosclerotic heart disease, cardiomyopathy, hypertension, major depressive disorder, transient
ischemic attack, and thoracic aortic ectasia.
Further review of the medical record and of the progress notes for Resident #66 revealed no documentation
of him expiring in the facility. The last health status note was dated [DATE] at 9:09 A.M. There was a
psychiatric progress note dated [DATE].
Review of a document titled Code Blue Bedside Documentation dated [DATE] and the Emergency Medical
Services run report dated [DATE], which were not part of the medical record and provided to the surveyor
upon request for an incident investigation, revealed Resident #66 expired in the facility on [DATE].
On [DATE] at 9:00 A.M. an interview with Registered Nurse (RN) #300 confirmed there was no
documentation in the medical record pertaining to the death of Resident #66.
This deficiency represents non-compliance investigated under Complaint Number OH00152130.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365667
If continuation sheet
Page 6 of 6