F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observations, record review, and interviews, the facility failed to implement the comprehensive care plan
related to adaptive devices for one (Resident #63) of 34 residents sampled for care plans.
Findings included:
The medical record review for Resident #63 revealed that the resident was admitted to the facility on [DATE]
with multiple diagnoses including but not limited to hemiplegia and hemiparesis following unspecified
cerebrovascular disease affecting the left non-dominant side with a contracture to the left hand/wrist. A
review of the resident's MDS (Minimum Data Set) dated 12/12/2020, section C for cognition, indicated that
the resident had a Brief Interview for Mental Status (BIMS) score of 11 out of 15 which indicated that her
memory was moderately impaired.
The plan of care for Resident #63 for range of motion, revealed that she had a risk of actual limitations as
evidenced by impairment on one side left hand/wrist date initiated 1/28/21. As an intervention the resident
should have an adaptive device: left hand wrist splint; apply to left hand.
A review of the physician's order read: remove before/after lunch or other, dated 1/28/2021. May remove for
skin sweep on 7-3.
A review of the MAR (Medication Administration Record) dated from 2/1/21 to 2/28/21 indicated that the
splint was applied after breakfast. One time a day monitor for redness, skin irritation, and discomfort. The
MAR indicated that Resident #63 had her hand splint applied 2/1, 2/2, and 2/3/21 at 9:00 a.m.
The observations were conducted throughout the survey as follows:
On 02/02/21 at 1:33 p.m., the resident did not have a splint on her left hand.
On 02/03/21 at 10:56 a.m., the resident was observed sleeping in bed with no splint on her left hand.
On 2/04/21 at 12:12 p.m., the resident did not have a splint on her left hand. She stated, the splint was in
her top drawer.
An interview was conducted with the resident's CNA (Certified Nursing Assistant) staff member D, he
stated he had not seen a splint for the resident. He was regularly assigned to the resident.
(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:
105286
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
105286
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/05/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bartow Center
2055 E Georgia St
Bartow, FL 33830
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
On 02/04/21 at 12:13 p.m., the NHA (Nursing Home Administrator) was advised of the finding and interview
with staff member D. The Treatment Administration Record (TAR) was reviewed for the month of February
2021 which indicated that the splint had been placed on the resident's left wrist at 9:00 a.m. for 2/1, 2/2 and
2/3/21 when in actuality the resident was observed with no splint throughout the survey.
On 02/04/21 at 12:54 p.m., an interview was conducted with the Director of Nursing regarding the facility's
expectation on accuracy of documentation. She explained that her expectation was not to document that a
splint was placed on a resident when it was not. Her expectation was to follow the plan of care for the
resident.
Event ID:
Facility ID:
105286
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
105286
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/05/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bartow Center
2055 E Georgia St
Bartow, FL 33830
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 0689
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interviews, record reviews, and review of facility policy, the facility did not ensure post fall neurological
checks were completed for one (Resident #234) of four residents sampled for falls.
Findings included:
A review of Resident #234's medical record revealed that he was admitted to the facility on [DATE] with
diagnoses of COVID-19, difficulty walking, and muscle weakness.
A review of the resident's care plan revealed that the resident was at risk for falls or fall related injury due to
deconditioning and gait/balance problems. Interventions included remind resident and reinforce safety
awareness, provide environmental adaptations, and anticipate and meet the resident's needs.
A review of the progress notes dated 02/01/2021 at 4:47 a.m., revealed that the resident was found on the
floor of his room, laying on his right side near the window around 2:15 a.m. He was assessed by the nurse
and had no complaints of pain or discomfort. The resident suffered a skin tear to the top of his right hand,
which was treated by the nurse. He was assisted back to bed and neurological checks were started.
An interview was conducted on 02/04/2021 at 2:10 p.m. with the facility's Risk Manager (RM). The RM
stated that the resident was found on the floor of his room by the window by staff. He was assessed by the
nurse following the fall and was found to have no injuries except for a small skin tear to the back of his right
hand. The resident was placed on neurological checks because the fall was not witnessed by staff. The RM
stated that she was not able to locate the neurological checks for Resident #234.
An interview was conducted on 02/04/2021 at 3:12 p.m. with the facility's Staff Development Coordinator
(SDC). The SDC stated that she was Resident #234's nurse when he fell on [DATE]. He had an
unwitnessed fall around 2:15 a.m. and was assessed for injuries after the fall. The resident had no apparent
injuries except for a small skin tear to the top of his right hand. The SDC stated that the resident was
started on neurological checks, which were continued throughout the shift and passed on to the next shift.
The SDC stated that Resident #234's neurological checks could not be located in the binder that they were
normally kept in.
An interview was conducted on 02/04/2021 at 4:07 p.m. with the facility's Director of Nursing (DON). The
DON stated that if a resident had an unwitnessed fall, neurological checks were started and the resident
would be assessed by the nurse to verify that there was no injury sustained. The DON also stated that
Resident #234's neurological checks could not be located in his chart or in the binder where they were
normally kept. The DON stated that neurological checks should have been started following the resident's
unwitnessed fall, but the record could not be located.
A review of the facility policy titled, Neurological Evaluation, dated February 2020, revealed that a
neurological assessment would be completed when a resident had experienced a change in level of
consciousness, after a fall with a known head injury, or after an unwitnessed fall.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105286
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
105286
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/05/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bartow Center
2055 E Georgia St
Bartow, FL 33830
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 0698
Provide safe, appropriate dialysis care/services for a resident who requires such services.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interviews, record reviews, and review of facility policy, the facility failed to provide post-dialysis assessment
to one (Resident #26) of one resident sampled for dialysis.
Residents Affected - Few
Findings included:
A review of Resident #26's medical record revealed that the resident was admitted to the facility on [DATE]
with diagnoses of End Stage Renal Disease and dependence on renal dialysis.
A review of the care plan revealed that the resident had renal failure and was on hemodialysis.
Interventions included communication and coordination with dialysis center regarding care plan goals,
observe for signs and symptoms of infection, injury at access site, and observe dialysis site for signs and
symptoms of bleeding.
A review of the Physician's Orders revealed an order, dated 02/02/2021, to document vital signs upon
returning from dialysis for monitoring.
A review of the Dialysis Communication Forms, dated 01/04/2021 and 01/06/2021, revealed under the
section titled, Facility Nurse Completes This Section:, no documentation. The sections for documenting the
resident's vital signs, assessment of access site, assessment of dressing, and mental status assessment
contained no documentation.
A review of the facility policy titled, Dialysis Management, dated February 2020, revealed under the section
Guidelines, that staff were to complete the Dialysis Communication Tool before and after dialysis and follow
up on any special instructions from the dialysis center. The policy also revealed that staff were to evaluate
for and manage post dialysis complications which may include, but were not limited to confusion, fever,
pruritus, anaphylaxis, seizures, hypotension, muscle cramps, cardiac arrhythmia, restlessness, air embolus,
insomnia, and hemorrhage.
An interview was conducted on 02/04/2021 at 4:24 p.m. with Staff G, Licensed Practical Nurse (LPN). Staff
G, LPN stated that the Dialysis Communication Tool was filled out by the nurse at the facility before the
resident left for dialysis and after the resident returned to the facility from dialysis. The facility nurse would
document an assessment of the dialysis site as well as assessment of vital signs upon return to the facility.
Staff G, LPN stated that all entries on the Dialysis Communication Tool should be filled in completely and
no areas of the form should be left blank.
An interview was conducted on 02/04/2021 at 4:35 p.m. with the Director of Nursing (DON). She stated that
the nurses complete the post dialysis assessments on the Dialysis Communication Tool when a resident
returned from dialysis. Nurse's should be filling out the form and documenting the assessments completely.
The DON stated that nursing staff should monitor the resident's dialysis site when they return to the facility
and document the assessment on the Dialysis Communication Tool.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105286
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
105286
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/05/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bartow Center
2055 E Georgia St
Bartow, FL 33830
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
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.
Based on observation, interview, and record review, the facility did not ensure that four vials of Lorazepam
2 mg/ml solution, a controlled substance, was kept in a separately locked, permanently affixed
compartment inside of the refrigeration unit.
Findings included:
On 2/04/21 at 11:50 a.m., the medication storage room for the 100 hall and 200 hall was observed with
Staff A, LPN. The medication room was entered, and immediately across from the door was a small
refrigerator. The refrigerator had a key lock on the left side. Staff A, LPN used a key to open the lock. Inside
the refrigerator was a large plastic container approximately eleven inches long, seven inches wide, and two
inches deep. Staff A, LPN said that this was the EDK (Emergency Drug Kit). Attached to the top of this
plastic box with hook and loop fasteners was another small plastic box that was the size of a standard deck
of playing cards that contained four vials of Lorazepam 2 mg/1 ml. The large plastic container was taken out
of the refrigerator and placed on the counter. The small plastic box containing the Lorazepam was easily
removed. Staff A, LPN then proceeded to open a gray metal lock box that was approximately seven inches
long and six inches wide that was permanently affixed to the shelving of the refrigerator. The shelving of the
refrigerator could not be removed. The lock box was empty.
Staff A, LPN confirmed that the small plastic box contained four vials of Lorazepam 2 mg/1 ml and that the
Lorazepam should have been placed in the locked box.
Staff A, LPN stayed in the medication room with the unlocked medications while a member of
administration could be located. Staff B, Regional Nurse, walked up and asked if she could be of
assistance. She walked into the medication room and was shown the EDK, which included the small box of
unsecured narcotics. She said, The lock box is right there.
Staff A, LPN took the unsecured narcotics, put them into the lock box, and locked it.
When asked what her expectation was of the narcotic refrigerated EDK, the regional nurse said it should be
in the lock box
At 12:55 p.m., in an interview with the DON (Director of Nursing), she said that refrigerated controlled
substances should be kept in a lock box.
In a policy and procedure given by the facility titled, Controlled Medication Storage dated 11/2017, the
policy read, Medications included in the Drug Enforcement Administration (DEA) classification as controlled
substances are subject to special ., storage Under procedures, #4 reads Controlled medications requiring
refrigeration are stored within a locked, permanently affixed box within the refrigerator.
Consultant Pharmacist interview was attempted without success on 2/05/2021 at 9:36 a.m. and 3:58 p.m.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105286
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
105286
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/05/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bartow Center
2055 E Georgia St
Bartow, FL 33830
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.
Based on observations, interviews, record review and policy review the facility failed to maintain a complete
and accurate medical record for one (Resident #63) of 34 sampled residents related to inaccurate
documentation for the application of a left hand splint.
Findings Included:
A review of the plan of care for Resident #63 for range of motion, revealed that she had a risk of actual
limitations as evidenced by impairment on one side left hand/wrist date initiated 1/28/21. As an intervention
the resident should have an adaptive device: left hand wrist splint; apply to left hand.
A review of the physician's order read: remove before/after lunch or other, dated 1/28/2021. May remove for
skin sweep on 7-3.
A review of the MAR (Medication Administration Record) dated from 2/1/21 to 2/28/21 indicated that the
splint was applied after breakfast. One time a day monitor for redness, skin irritation, and discomfort. The
MAR indicated that Resident #63 had her hand splint applied 2/1, 2/2, and 2/3/21 at 9:00 a.m.
The observations were conducted throughout the survey as follows:
On 02/02/21 at 1:33 p.m., the resident did not have a splint on her left hand.
On 02/03/21 at 10:56 a.m., the resident was observed sleeping in bed with no splint on her left hand.
On 2/04/21 at 12:12 p.m., the resident did not have a splint on her left hand. She stated, the splint was in
her top drawer.
An interview was conducted with the resident's CNA (Certified Nursing Assistant) staff member D, he
stated he had not seen a splint for the resident. He was regularly assigned to the resident.
On 02/04/21 at 12:13 p.m., the NHA (Nursing Home Administrator) was advised of the finding and interview
with staff member D. The Treatment Administration Record (TAR) was reviewed for the month of February
2021 which indicated that the splint had been placed on the resident's left wrist at 9:00 a.m. for 2/1, 2/2 and
2/3/21 when in actuality the resident was observed with no splint throughout the survey.
On 02/04/21 at 12:54 p.m., an interview was conducted with the Director of Nursing regarding the facility's
expectation on accuracy of documentation. She explained that her expectation was not to document that a
splint was placed on a resident when it was not. Her expectation was to follow the plan of care for the
resident.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105286
If continuation sheet
Page 6 of 6