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, record review, resident and staff interview, the facility failed to provide a call light to
accommodate the needs, of 1 (Resident #108) of 5 residents reviewed for call light needs.
Residents Affected - Few
The findings included:
Review of the clinical record revealed Resident #108 was admitted to the facility on [DATE] with diagnoses
including quadriplegia (paralysis of all four limbs).
The admission Minimum Data Set (MDS) assessment with an assessment reference date of 12/22/22
noted the resident required extensive physical assistance of two persons for all activities of daily living,
including bed mobility and transfer.
On 2/19/23 at 10:16 a.m., Resident #108 was observed in bed. A flat pad call light (specialized call light for
residents with limited dexterity activated by slight pressure) was on the floor, not accessible to the resident.
Resident #108 said, I can't use it anyway.
On 2/20/23 at 9:02 a.m., Resident #108 was observed in bed. A flat pad call light was on a pillow by the
resident's right shoulder. Resident #108 said she could not activate the call light. She said, I don't have the
strength.
Registered Nurse (RN) Staff R was present during the observation. She said she didn't know it the resident
could activate the call light. RN Staff R said Resident #108 could benefit from a puff call light (specialized
call light activated by a sip or blow puff into a straw like wand).
On 2/20/23 at 9:04 a.m., Certified Nursing Assistant (CNA) Staff P said she was assigned to Resident
#108. She said the resident had the flat pad call light and, hits it with her chin. CNA Staff P said Resident
#108 did not usually use the call light, she just calls out when she needs something. CNA Staff P said she
just leaves the door open for Resident #108 to call out when she needs something.
On 2/21/23 at 8:45 a.m., Resident #108 was observed in bed with a puff call light to the left of her face.
Resident #108 said she was very happy to have a call light that she could use to call for assistance when
needed.
On 2/22/23 at 11:20 a.m., the Administrator verified Resident #108 had been at the facility for two months.
He said Resident #108 should have had a blow bell right away to meet her needs.
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:
105342
Printed: 05/28/2026
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
105342
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Rehab & Healthcare Center of Cape Coral
2629 Del Prado Blvd
Cape Coral, FL 33904
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
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 staff interview the facility failed maintain an indwelling catheter
(tube inserted into the bladder to drain urine) in a safe and sanitary manner for 1(Resident #69) of 1
resident sampled with an indwelling catheter. This had the potential to cause urinary tract infection and
complications.
The findings included:
Review of the clinical record revealed Resident #69 had an admission date of 9/19/22 with diagnoses
including dementia, epilepsy and hemiplegia affecting the left side, urinary tract infections and neurogenic
bladder (lack of bladder control due to brain, spinal cord, or nerve problem).
The Quarterly Minimum Data Set (MDS) (standardized assessment tool that measures health status in
nursing home residents) with an assessment reference date of 12/21/22 documented Resident #69
required extensive assistance with transfers and bed mobility.
The MDS noted Resident #69's cognition was intact.
The care plan initiated on 9/19/22 documented the Resident uses a urinary catheter with risk for infection
and or complication.
The care plan goal specified to minimize the risk of complications associated with catheter usage. The care
plan interventions specified, provide catheter care daily and as needed, and keep drainage bag (collects
urine from the catheter) below level of bladder.
Observations on 2/19/23 at 9:53 a.m., 11:24 a.m., and 3:47 p.m., Resident #69 was in bed. The urinary
catheter drainage bag was lying on the floor next to the bed.
Photographic evidence obtained.
On 2/20/23 at 8:29 a.m., during an observation with Registered Nurse (RN) Staff R, the urinary catheter
drainage bag for Resident #69 was lying on the floor next to the bed. RN Staff R confirmed the observation
and said the urinary drainage bag should be positioned off the floor.
On 2/21/23 at 11:30 a.m., the Regional Nurse Consultant said the facility had no policy regarding catheter
drainage bags or care.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105342
If continuation sheet
Page 2 of 6
Printed: 05/28/2026
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
105342
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Rehab & Healthcare Center of Cape Coral
2629 Del Prado Blvd
Cape Coral, FL 33904
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 0700
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Try different approaches before using a bed rail. If a bed rail is needed, the facility must (1) assess a
resident for safety risk; (2) review these risks and benefits with the resident/representative; (3) get informed
consent; and (4) Correctly install and maintain the bed rail.
Based on observation, record review, review of facility policy, and staff interviews, the facility failed to
ensure 1(Resident #69) of 1 resident reviewed for accidents was assessed for alternative interventions prior
to the use of bed rails. The facility failed to review the risks and benefits of bed rails with the resident or
resident representative and obtain informed consent prior to installation. In addition, the facility failed to
have ongoing routine maintenance of the bed rails to ensure they remained safe for resident's use.
The findings included:
The facility policy Side Rail-Assistive Device (effective 10/21) documented, Side rails will not be used
unless or until all other alternative devices have been exhausted. If a side rail is used the facility must
ensure correct installation, use and maintenance of rail. Side rails may be a restraint or entrapment risk.
Side rails will not be used as a restraint. The facility strives to ensure the safety of residents by following
manufacturer's instructions and through preventive maintenance of side rails. Facility will maintain a list of
residents utilizing side rails as assistive devices and will routinely audit for appropriate usage, safety and
function. Assistive device: Any item used by, or in the care of the resident to promote, supplement, or
enhance resident function and or safety. Side rails: include rails of various sizes.
Review of the clinical record revealed Resident #69 had an admission date of 9/19/22 with diagnoses
including dementia, epilepsy (seizure) and hemiplegia (paralysis) affecting the left side.
The Quarterly Minimum Data Set (MDS) (standardized assessment tool that measures health status in
nursing home residents) with an assessment reference date of 12/21/22 documented Resident #69
required extensive assistance with transfers and bed mobility.
The MDS noted Resident #69's cognitive skills for daily decision making was intact.
On 2/19/23 at 3:41 p.m., Resident #69 was observed in a low bed, on an air mattress with inflatable sides.
The bed had grab bars in the raised position on both sides of the bed. Resident #69 said he did not know
what a grab bar was and was not observed using the device.
Further review of the clinical record for Resident #69 revealed no documentation of signed consent or
alternative interventions attempted prior to the use of the grab bars.
On 2/22/23 at 8:25 a.m., the Regional Nurse Consultant (RNC) said she was not able to locate a consent
or documentation of alternative interventions before the use of grab bars for Resident #69. The RNC said, it
was her understanding grab bars were not considered side rails.
The RNC said therapy usually assesses a resident for grab bars, but she found no documentation that
therapy assessed the resident prior to the use of the grab bars.
The facility failed to provide requested documentation of routine maintenance including assessment of
entrapment for use of the grabs used for Resident #69.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105342
If continuation sheet
Page 3 of 6
Printed: 05/28/2026
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
105342
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Rehab & Healthcare Center of Cape Coral
2629 Del Prado Blvd
Cape Coral, FL 33904
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 0732
Post nurse staffing information every day.
Level of Harm - Potential for
minimal harm
Based on observation and staff interview, the facility failed to post the required current daily staffing data in
a prominent place readily accessible to residents and visitors.
Residents Affected - Some
The findings included:
On 2/19/2023 at 11:21 a.m., the facility daily staffing was posted and reflected a current census of 114 for
2/19/2023.
On 2/20/2023 at 7:29 a.m., the facility daily staffing posted and remained dated as 2/19/23 but the census
was changed to 111.
On 2/20/23 at 3:38 p.m., the facility daily staffing was not updated and remained dated as of 2/19/23.
On 2/22/23 at 12:25 p.m., the facility daily staffing was not updated and remained dated 2/19/23 with a
census of 111.
On 2/22/23 at 12:30 p.m., the administrator stated the staffing coordinator was responsible for posting and
updating the staffing numbers. He said The process needed to be posted and updated daily for all visitors
or residents to view at the receptionist desk.
The administrator stated the staffing should reflect today's date and verified the staff information posted
was from 2/19/23.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105342
If continuation sheet
Page 4 of 6
Printed: 05/28/2026
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
105342
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Rehab & Healthcare Center of Cape Coral
2629 Del Prado Blvd
Cape Coral, FL 33904
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 0756
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart,
following irregularity reporting guidelines in developed policies and procedures.
Based on a review of the Consultant Pharmacist's Medication Regimen Review report, and staff interview,
the facility failed to have documentation of monthly medication review for 2 (Resident #93, and #27) of 5
residents sampled for unnecessary medication review.
The findings included:
Review of the facility policy Medication Monitoring Section 8.1 Medication Regimen Review (MRR) and
Reporting dated 09/18 Procedures:
The consultant pharmacist reviews the medication regimen and medical chart of each resident at least
monthly .
The findings are communicated to the Director of Nursing (DON) or designee and the medical director. The
findings are documented and filed with other consultant pharmacist recommendations in the resident's
chart.
Resident specific MRR recommendations and findings are documented and acted upon by the nursing care
center and/or physician.
A record of the consultant pharmacist's recommendations is made available .within 48 hours of completion.
The nursing care center follows-up on the recommendations to verify that appropriate action has been
taken. Recommendations shall be acted upon within 30 calendar days.
1. Review of Resident #27's clinical record revealed an admission date of 6/14/22. The resident remained at
the facility without discharge or transfer to the hospital.
Review of the Consultant Pharmacist's Medication Regimen Review from 6/2022 through January 2023
failed to show documentation the Consultant Pharmacist reviewed Resident #27's medication regimen in
September 2022 or January 2023.
2. Review of the clinical record for Resident #93 revealed an admission date of 8/17/22. Resident #93
remained at the facility without discharges or transfer to the hospital.
Review of the Consultant Pharmacist's Medication Regimen Review from 8/2022 through January 2023
failed to show documentation the Consultant Pharmacist reviewed Resident #93's medication regimen in
December 2022.
On 2/22/23 at 10:00 a.m., the DON said he could not locate documentation the Consultant Pharmacist
reviewed the Medication Regimen for Resident #27 in July 2022 or January 2023. He said he did not have
documentation of Medication Regimen Review for Resident #93 for December 2022.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105342
If continuation sheet
Page 5 of 6
Printed: 05/28/2026
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
105342
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Rehab & Healthcare Center of Cape Coral
2629 Del Prado Blvd
Cape Coral, FL 33904
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 - Some
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 record review, the facility failed to remove outdated medications from the
refrigerator and failed to ensure proper storage of medications to prevent unauthorized access for 1 (Unit 2)
of 2 units observed.
The findings included:
The Facility policy titled: Medication Storage, Section 4.1, dated 9/18, was provided.
The policy stated the medication supply shall be accessible only to licensed nursing personnel, pharmacy
personnel or staff members lawfully authorized to administer medications.
Procedure #3 indicated in order to limit access to prescription medications, only licensed nurses, pharmacy
staff, and those lawfully authorized to administer medications are allowed access to medication carts.
Medication rooms, cabinets, and medication supplies should remain locked when not in use or attended by
persons with authorized access.
Procedure #14 indicated outdated, contaminated, discontinued, or deteriorated medications, and those in
containers that are cracked, soiled or without secure closures are immediately removed from stock, and
disposed of according to procedures for medication disposal.
1. On [DATE] at 12:30 p.m., observation of Unit 2 medication storage room refrigerator with Licensed
Practical (LPN) Staff A revealed two pre-drawn tubersol (test to diagnose tuberculosis infection) syringes
expired [DATE], and [DATE].
LPN Staff A verified the tubersol syringes were expired and said she would discard them.
2. On [DATE] at 10:32 a.m., an opened box containing seven bottles of medications was observed on the
counter of Unit 2's nurse's station.
Registered Nurse Staff D closed the box, placed a 3-hole puncher and stapler on the box and walked away
from the nurse's station, leaving the box of medications unattended and accessible to residents, visitors
and unauthorized staff.
3. On [DATE] at 10:46 a.m., the administrator came to unit 2 nursing station and verified the box of
medication was unattended at the nurse's station. He removed the box and stated he would take it to the
Director of Nursing (DON).
On [DATE] at 3:43 p.m., the DON said he needed to remind and educate staff to lock medication and
treatment carts.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105342
If continuation sheet
Page 6 of 6