F 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate
catheter care, and appropriate care to prevent urinary tract infections.
Based on observation, record review and interview the facility failed to ensure Resident #3's indwelling
Foley catheter (a thin sterile tube inserted into the bladder to drain urine) bag was emptied properly to
prevent potential complications for the resident. This affected one resident (#3) of one resident reviewed for
catheters.
Findings include:
Review of the medical record for Resident #3 revealed an admission date of 11/24/19 with diagnoses
including chronic respiratory failure, chronic kidney disease, neuromuscular dysfunction of the bladder,
benign prostatic hyperplasia with lower tract symptoms and spinal stenosis.
Review of the care plan, dated 11/25/19 revealed Resident #3 required alternate means of urinary
elimination of a Foley catheter due to neurogenic bladder, benign prostatic hyperplasia with lower urinary
tract symptoms, urinary tract infection and sepsis. Interventions included catheter care every shift and as
needed, monitor catheter patency every shift, position drainage bag below the level of the bladder and
keeping the bag and tubing off the floor always. There was nothing in the care plan regarding emptying the
catheter drainage bag.
Review of physician's orders for March 2020 revealed Resident #3 had an order for an indwelling Foley
catheter to continuous drainage and catheter care every shift. There were no physician orders regarding
emptying the Foley catheter drainage bag.
Observation on 03/02/20 at 11:29 A.M. revealed Resident #3's indwelling Foley catheter drainage bag
laying on the floor while Resident #3 was in bed. Resident #3's catheter drainage bag was all the way full of
urine and the urine was backing up into the catheter tubing. His drainage bag was leaking out the bottom of
the catheter bag and the bag was laying in a puddle of urine.
Interview and observation with the Director of Nursing on 03/02/20 at 11:32 A.M. verified the indwelling
Foley catheter bag was overfull causing the urine to back up into the catheter tubing as well as leak out of
the bottom of the catheter bag. She verified the catheter bag should have been emptied and not had this
amount of urine in the bag. The Director of Nursing emptied the urinary catheter bag and measured the
urine content and she revealed the urinary output measured 3000 cubic centimeters (cc).
Review of manufacturer guidelines, SteriGear the Fig Leaf with a model number of 10270 revealed
Resident #3's urinary drainage bag had a capacity of 2000 milliliters. The guidelines revealed to hang the
bag utilizing the hanger or rope and do not place the bag on the floor. The guidelines also
(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:
366326
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
366326
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/05/2020
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Geneva Center for Rehabilitation and Nursing
1140 South Broadway
Geneva, OH 44041
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 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
revealed to periodically check the fluid level in the bag by lifting the Fig Leaf cover or by viewing through the
Quick View Port and empty the bag.
Review of facility policy titled, Catheter Care, Urinary dated 05/22/13 revealed it was the policy of the facility
to provide appropriate care for urinary catheters and to prevent catheter- associated urinary tract infections.
The policy revealed to be sure the catheter tubing and drainage bag were kept off the floor and empty the
drainage bag regularly using a separate clean collection container for each resident. The policy revealed
the bag should be emptied at least every eight hours.
Event ID:
Facility ID:
366326
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
366326
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/05/2020
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Geneva Center for Rehabilitation and Nursing
1140 South Broadway
Geneva, OH 44041
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
Based on observation, record review and interview the facility failed to maintain a medication rate less than
five percent. The facility medication error rate was calculated to be 12.90% and included four medication
errors out of 31 medication administration opportunities. This affected one resident (#43) of five residents
observed for medication administration.
Residents Affected - Few
Findings include:
Review of the medical record for Resident #43 revealed an admission date of 01/23/20 and diagnoses
including gastro-esophageal reflux disease, hypertension, hypokalemia (low potassium), chest pain and
major depression.
Review of Resident #43's quarterly Minimum Data Set (MDS) 3.0 assessment, dated 02/12/20 revealed
she had intact cognition.
Observation on 03/03/20 at 8:25 A.M. of medication administration for Resident #43 completed by Licensed
Practical Nurse (LPN) #600 revealed Resident #43 requested her medication be crushed and placed in
applesauce. LPN #600 crushed all Resident #43's medications including Cymbalta capsule delayed release
30 milligrams one capsule by mouth for major depression, Isosorbide mononitrate tablet extended release
30 milligram by mouth for chest pain, Pantoprazole sodium delayed release 40 milligram tablet by mouth for
gastro-esophageal reflux and Potassium chloride extended release 20 milliequivalent tablet by mouth for
hypokalemia (low potassium). LPN #600 did not educate Resident #43 prior to administering the delayed
release or extended release medication on risk factors of these medications being crushed or call the
physician prior to these medications being crushed and administered.
Interview on 03/03/20 at 8:30 A.M. with LPN #600 verified she crushed all of Resident #43's medications
including her Cymbalta delayed release, Isosorbide mononitrate extended release, Pantoprazole sodium
delayed release and her Potassium chloride extended release. She verified these medications should not
have been crushed and she revealed she should have called the physician prior to crushing the
medications and administering.
Interview on 03/03/20 at 9:55 A.M. with Facility Pharmacist #601 verified Resident #43's Cymbalta delayed
release, Isosorbide mononitrate extended release, Pantoprazole sodium delayed release and her
Potassium chloride extended should not be crushed as extended release medications were formulated for a
resident to receive the medication slowly over time and delayed release medications were enteric coated
designed to delay the release of the medication until the tablet had passed through the stomach to prevent
the medication from being destroyed or inactivated by gastric juices or where it may irritate the gastric
lining.
Review of facility policy titled Medication Administration- Crushing of Medications, dated 06/21/17 revealed
medications which were enteric coated, extended release, sublingual or otherwise noted by the
manufacturer as inappropriate to crush, may not be crushed. If crushing of the medication was authorized
by the physician, the pharmacy should be notified, and documentation must be made in the resident's
record. If the physician orders the crushing of a Do Not Crush medication the physician must document in
the resident's chart to indicate that the benefits of crushing the medication outweigh the risk of crushing the
medication.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366326
If continuation sheet
Page 3 of 3