F 0686
Provide appropriate pressure ulcer care and prevent new ulcers from developing.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observations, interviews, and record reviews, the facility failed to ensure residents received care and
treatment consistent with professional standards of practice to promote healing and to prevent further
development of skin breakdown or pressure ulcers for two (Resident #10 and Resident #32) of five
residents reviewed for pressure ulcers.
Residents Affected - Some
1.
The facility failed to ensure Resident #10 was repositioned every two hours as indicated in Resident #10's
physician orders.
2.
The facility failed to ensure Resident #32 was repositioned every two hours as indicated in Resident #32's
care plan.
These failures could place residents at risk for worsening pressure ulcers, new pressure ulcers, or infection.
Findings included:
1.
Record review of Resident #10's Annual MDS assessment dated [DATE] revealed Resident #10 was an
[AGE] year-old female admitted to the facility on [DATE] and diagnoses included malnutrition, pressure
ulcer of sacral region (lower back and upper buttocks), muscle wasting and muscle atrophy (decrease of
muscle mass). Section C of the MDS indicated Resident #10's BIMS was 00 (indicated severe cognitive
impairment). Section GG of Resident #10's MDS indicated Resident #10 was dependent (required
assistance and was unable to help with activities) with all ADLs and was unable to roll to the left or right.
Section M of Resident #10's MDS assessment indicated Resident #10 was at risk for developing pressure
ulcers.
Record review of Resident #10's care plan with a revision date of 1/13/2025 revealed Resident #10 had the
potential to develop pressure ulcers and interventions included to reposition the resident frequently or more
often as needed.
Record review of Resident #10's wound evaluation and summary report dated 2/18/2025 revealed Resident
#10's wound on her sacrum was healed and the wound had been present for more than 364 days.
(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 11
Event ID:
675057
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 0686
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Record review of Resident #10's physician order dated 3/03/2025 revealed Resident #10 should be
repositioned every two hours.
In an observation on 3/04/2025 at 10:46 a.m., Resident #10 was observed laying flat on her back with one
pillow under her head. No other pillows or wedges (foam wedge used for positioning) were observed in
Resident #10's room. Resident #10 was unable to answer questions appropriately.
In an observation on 3/04/2025 at 1:24 p.m., Resident #10 was observed in the same position on her back
with one pillow under her head. No other pillows or wedges were observed in Resident #10's room.
In an observation on 3/05/2025 at 11:05 a.m., Resident #10 was observed in the same position on her back
with one pillow under her head. No other pillows or wedges were observed in Resident #10's room.
In an observation on 3/05/2025 at 1:49 p.m., Resident #10 was observed in the same position on her back
with one pillow under her head. No other pillows or wedges were observed in Resident #10's room.
In an observation on 3/05/2025 at 3:36 p.m., Resident #10 was observed in the same position on her back
with one pillow under her head. No other pillows or wedges were observed in Resident #10's room.
In an observation on 3/06/2025 at 9:00 a.m., Resident #10 was observed in the same position on her back
with one pillow under her head. No other pillows or wedges were observed in Resident #10's room.
Record review of Resident #10's progress note dated 3/03/2025 at 1:54 p.m. by RN B, revealed an open
area was noted to the coccyx (area near the top of the buttocks and the base of the spine). Measurements
or wound type were not indicated.
In an interview on 3/06/2025 at 2:30 p.m., ADON C stated the measurements for Resident #10's new
wound was 0.5 x 0.5 cm. The doctor and hospice were notified on 3/03/2025. ADON C stated it was an
open area and did not indicate the specific type of wound.
2.
Record review of Resident #32's Quarterly MDS assessment dated [DATE] revealed Resident #32 was a
[AGE] year-old female admitted to the facility on [DATE] with diagnoses of diabetes, aphasia (inability to
comprehend of formulate language), hemiplegia (partial paralysis of one side of the body) or hemiparesis
(muscle weakness of one side of the body), and muscle wasting and muscle atrophy (decrease of muscle
mass). Section C of the MDS assessment also revealed Resident #32 had severely impaired cognitive skills
and was rarely/never understood. Section GG of Resident #32's MDS indicated Resident #32 was
dependent (required assistance and was unable to help with activities) with all ADLs and was unable to roll
to the left or right without assistance. Section M of Resident #32's MDS assessment indicated Resident #32
had one stage 4 pressure ulcer that was present upon admission and had not healed at the time of the
assessment.
Record review of Resident #32's care plan with a revision date of 2/06/2025 revealed Resident #32
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 2 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 0686
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
had a pressure ulcer, and interventions included to reposition the resident every two hours or more often as
needed or requested.
Record review of Resident #32's wound evaluation and summary report dated 1/28/2025 revealed Resident
#32 had a wound on her sacrum for more than 203 days with measurements of 4 x 2.5 x 1cm.
Recommendations included to reposition per facility protocol and turn side to side in bed every one to two
hours if able.
Record review of Resident #32's wound evaluation and summary report dated 2/25/2025 revealed Resident
#32 had a wound on her sacrum for more than 231 days with measurements of 4 x 2.5 x 1cm.
Recommendations included to reposition per facility protocol and turn side to side in bed every one to two
hours if able.
In an observation on 3/04/2025 at 10:49 a.m., Resident #32 was observed lying flat on her back with two
wedges observed stuck between the bed and the wall. One pillow was placed under the resident's head.
Resident #32 was unable to answer questions due to a severe cognitive impairment.
In an observation on 3/04/2025 at 1:26 p.m., Resident #32 was observed in the same position lying flat on
her back with two wedges observed stuck between the bed and the wall. One pillow was placed under the
resident's head.
In an observation on 3/05/2025 at 10:58 a.m., Resident #32 was observed in the same position lying flat on
her back with one wedge observed next to the resident on her right side (not under). Another wedge was
observed stuck between the bed and the wall. One pillow was placed under the resident's head.
In an observation on 3/05/2025 at 1:48 p.m., Resident #32 was observed in the same position lying flat on
her back with one wedge observed next to the resident on her right side (not under). Another wedge was
observed not placed under the resident and lying on the foot of the bed.
In an observation on 3/05/2025 at 3:38 p.m., Resident #32 was observed in the same position lying flat on
her back with one wedge observed next to the resident on her right side (not under). Another wedge was
observed not placed under the resident and lying on the foot of the bed.
In an observation on 3/06/2025 at 9:00 a.m., Resident #32 was observed in the same position lying flat on
her back with one wedge observed next to the resident on her right side (not under). The other wedge was
no longer in the room.
In an interview on 3/05/2025 at 4:08 p.m., CNA A reported that pressure sores were prevented by rotating
or turning the resident every two hours. CNA A stated some residents had extra pillows, and some
residents had wedges to use for turning. CNA A stated that if a resident was not turned then sores could
develop. CNA A stated Resident #32 and Resident #10 were turned every two hours to prevent sores from
developing.
In an interview on 3/06/2025 at 10:10 a.m., RN B reported if a resident was bedridden then they were
repositioned every one to two hours. RN B reported they used pillows to help reposition residents, and the
nurse was responsible for ensuring residents were repositioned. RN B stated if residents were not
repositioned then it could cause skin breakdown (wounds). RN B stated Resident #10 was on an air
mattress and was repositioned every one to two hours. RN B reported Resident #10 had wounds that
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 3 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 0686
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
did better some days and were worse on other days. RN B reported Resident #32 was repositioned with
wedges, but she was not sure how often. RN B stated the wedges lifted Resident #32's bottom off the bed.
RN B reported she was unsure if Resident #32's wounds had become worse because she had only worked
at the facility for around six weeks.
In an interview on 3/06/2025 at 11:16 a.m., ADON C stated Resident #10's wound was resolved, and
Resident #10 had just developed a new wound. ADON C stated the wound care doctor monitored the
status of wounds every Tuesday and documented any changes in the wound evaluation and summary
report. ADON C stated Resident #32's wound would never heal because Resident #32 was receiving a low
amount of nutrition via a tube feeding. ADON C reported Resident #32's wound was chronic and had not
changed significantly. ADON C reported the dietician was monitoring Resident #32, and Resident #32 was
unable to tolerate the tube feeding if it were increased. ADON C reported that Resident #32 and Resident
#10 should have been repositioned every two hours and as needed. ADON C stated pillows and wedges
were used for repositioning, and if residents were not repositioned then it could cause a pressure ulcer to
form or reopen. ADON B reported that the nurses were responsible for monitoring if residents were turned
every two hours.
In an interview on 3/06/2025 at 11:55 a.m., the DON reported that dependent (requires assistance)
residents should be turned everyone and a half to two hours and more frequently if they were in pain. The
DON stated pillows or wedges were used for repositioning the residents. The DON stated Resident #10 was
on hospice and wounds were not unexpected. The DON reported Resident #10 should still be repositioned
every one to two hours. The DON reported Resident #32 had a wound and should be repositioned every
one to two hours. The DON reported the nurses should monitor if residents were turned, and ADON C
monitored the wound documentation to determine if wounds were progressing.
Record review of facility's policy titled, Skin Management Policy, with a revision date of 2/01/2014, revealed
If new skin alterations of any type are identified .physician orders are obtained. The patient is reviewed by
the interdisciplinary team and a plan of care is initiated.
A policy specific to repositioning residents for pressure ulcer prevention was not received at the time of exit.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 4 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 - Some
Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart,
following irregularity reporting guidelines in developed policies and procedures.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review and interview, the facility failed to ensure any drug regimen irregularities reported by the
Pharmacist Consultant were acted upon for two (Residents #19 and Resident #9) out of six residents and
failed to ensure the Pharmacist Consultant reported irregularities to the Physician whose medications were
reviewed.
1.
Resident 19's Pharmacist consultant recommendation for a gradual dose reduction of Citalopram
(antidepressant medication) had no physician rationale for continued use.
2.
Resident 19's Pharmacist consultant recommendation for a gradual dose reduction of Quetiapine
(antipsychotic medication) had no physician rationale for continued use.
3.
Resident 9's Pharmacist consultant recommendation for a gradual dose reduction of Risperidone
(antipsychotic medication) had no physician rationale for continued use.
4.
Resident 9's Pharmacist consultant recommendation for a gradual dose reduction of Divalproex
(antipsychotic medication) had no physician rationale for continued use.
These failures could place residents at risk for adverse consequences and could cause a decline in their
physical, mental, and psychosocial condition.
Findings included:
Resident #19
Record review of Resident #19's face sheet dated 03/06/2025 reflected a [AGE] year-old male who was
admitted to the facility on [DATE] and re admitted on [DATE] with diagnoses which included Alzheimer's
Disease, schizoaffective disorder, and dysphagia (difficulty swallowing).
Record review of Resident #19's MDS assessment dated [DATE] revealed he had a BIMS score of 14
which indicated intact cognition. Resident #19 diagnoses included anxiety disorder, psychotic disorder, and
schizophrenia. Resident #19 received antipsychotic and antidepressant medications and exhibited no
behavioral symptoms.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 5 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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
Record review of Resident #19's care plan dated 01/17/2025 revealed Resident #19 had a psychosocial
well being problem r/t anxiety, schizophrenia, and depression. Goal: the resident will verbalize feelings
related to emotional state .the resident will identify appropriate diversional activities. Interventions: give
medication as ordered and monitor for side effects. Give positive reinforcement as initiative/involvement
improves/attempts to solve conflict. Monitor/document resident's usual response to problems.
Residents Affected - Some
Record review of Consultant Pharmacist Recommendation to Physician dated 10/31/2024 reflected: Dear
Physician G, Resident #19 has been taking Citalopram 10mg QAM 04/23/2024 without a GDR. Could we
attempt a dose reduction at this time to verify this resident is on the lowest possible dose? If not, please
indicate response below. The recommendation letter was not signed by Resident #19's Physician. There
was no rationale documented for GDR of Citalopram.
Record review of Consultant Pharmacist Recommendation to Physician dated 11/30/2024 reflected
Dear Physician G, Resident #19 has been taking Quetiapine 50mg BID since 03/10/2024 without a GDR.
Could we attempt a dose reduction at this time perhaps Quetiapine 25mg QAM and 50mg verify this
resident is on the lowest possible dose? If not, please indicate response below. The recommendation letter
was not signed by Resident #19's Physician. There was no rationale documented for GDR of Quetiapine.
Record review of Resident #19's Physician orders dated 04/23/2024 by Physician G for Citalopram 20mg.
Give one tablet by mouth in the morning for depression.
Record review of Resident #19's Physician orders dated 03/10/2024 by Physician G for Quetiapine 50mg.
Give one tablet by mouth two times a day related to schizophrenia. Dementia.
Review of Resident #19's electronic record revealed there was no documentation a rationale for continuing
the medications and not doing a GDR by the physician for Citalopram or Quetiapine.
In an interview on 03/06/25 at 12:08 PM Interview with Resident #19 stated he take medication for gout,
Motrin, and allergy medications. He stated he did not take any anti-depressants or any psychotropic
medications. He stated he did not have any changes to his medications.
Resident #9
Record review of Resident #9's face sheet dated 03/06/2025 reflected a [AGE] year-old male who was
admitted to the facility on [DATE] and readmitted [DATE] with diagnosis of schizophrenia, and major
depressive disorder.
Record review of Resident #9's MDS assessment dated [DATE] revealed he had a BIMS score of 15 which
indicated intact cognition. Resident #9 diagnosis included depression and schizophrenia. Resident #9
received antipsychotic medications and exhibited no behavioral symptoms.
Record review of Resident #9's care plan dated revealed Resident #9 used psychotropic medications
related to depression, schizophrenia. Goal: resident will maintain the highest level of function possible and
not experience a decrease in functional abilities related to psychotropic drug use during the next 90 days.
The resident will reduce the use of psychoactive medication over the next 90 days. Interventions: administer
medications as ordered. Monitor/document for side effects and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 6 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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
effectiveness.
Level of Harm - Minimal harm
or potential for actual harm
Record review of Consultant Pharmacist Recommendation to Physician dated 01/31/2025 reflected
Residents Affected - Some
Dear Physician G, Resident #9 has been taking Divalproex 500mg BID since 07/03/2024 without a GDR.
Could we attempt a dose reduction at this time to perhaps Divalproex 250mg QAM and 500mg to verify this
resident is on the lowest possible dose? If not, please indicate response below. The recommendation letter
was not signed by Resident #9's Physician. There was no rationale documented for GDR of Divalproex.
Record review of Consultant Pharmacist Recommendation to Physician dated 09/30/2024 reflected
Dear Physician G, Resident #9 has been taking Risperidone 2mg BID since 02/06/2024 without a GDR.
Could we attempt a dose reduction at this time to perhaps Risperidone 1mg QAM and 2mg to verify this
resident is on the lowest possible dose? If not, please indicate response below. The recommendation letter
was not signed by Resident #9's Physician. There was no rationale documented for GDR of Risperidone.
Record review of Resident #9's Physician orders dated 02/07/2024 by Physician G for Risperidone 2mg.
Give one tablet by mouth twice daily for schizophrenia.
Record review of Resident #9's Physician orders dated 07/04/2024 by Physician G for Divalproex 500mg.
Give one tablet by mouth twice daily for schizophrenia.
Review of Resident #9's electronic record revealed there was no documentation a rationale for continuing
the medications and not doing a GDR by the physician for Risperidone or Divalproex.
In an interview on 03/06/25 at 12:04pm with Resident #9 stated he took lisinopril and risperidone. He stated
was unsure what dosage took but he took the same medication daily in the morning and evening. He stated
he could not recall if he ever had a dosage reduction for any of his medications.
In an interview on 03/06/2025 at 9:10am with the DON she stated she's been employed at the facility for 4
weeks. She stated she is unsure what the process was for the pharmacist recommendations. She stated
since she's been in her position, she retrieved the pharmacist recommendations from the portal that she
only had access to and send the recommendations to the physician. She stated she faxed the
recommendations to the physician and the physician would review and sign the recommendations via fax or
in person.
In an interview on 03/06/2025 at 9:57am with the ADON she stated she's been employed at the facility
since October 2024. She stated she was the interim DON prior to the current DON being hired. She stated
when she was interim DON, she retrieved the pharmacist recommendations from the portal and send the
recommendations to the physician. She stated the physician reviewed and signed the recommendations
when she visited the facility once a week. She stated she tried retrieving the older pharmacist
recommendations that included the physician's signature, but she was unable to retrieve the
recommendations because the facility no longer had access to the prior DON's email. She stated she
contacted Physician G and the physician stated she received pharmacist recommendations from the prior
DON and reviewed, signed, and returned the recommendations to the facility. (The recommendations were
not provided prior to exit.)
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 7 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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
In an interview on 03/06/2025 at 11:11am with Physician G she stated she visited the facility weekly. She
stated the facility provided her copies of the pharmacist recommendations via email or in person when she
visited. She stated after she reviewed and signed the recommendations she returned the forms to the
facility. She stated once she returned the forms to the facility, she was unsure what the facility did with the
forms once received from her.
Residents Affected - Some
Record review of the facility's Unnecessary Drugs policy dated 10/24/2022 reflected, Policy Statement: It is
the facility's policy that each resident's drug regiment is managed and monitored to promote or maintain the
resident's highest practicable mental, physical, and psychosocial well-being free from unnecessary drugs.
2. The attending physician will assume leadership in medication management by developing, monitoring,
and modifying the medication regimen in collaboration with the resident and/or representatives, other
professionals, and interdisciplinary team. Each resident's drug regimen will be reviewed on an ongoing
basis, taking into consideration the following elements: A. dose(including duplicate therapy) B. Duration of
use C. Indications and clinical need for medication D. Adequate monitoring for efficacy and adverse
consequences E. Preventing, identifying and responding to adverse consequences F. Any combination of
reasons stated above.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 8 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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.
Based on observation, interview, and record review the facility failed to ensure all drugs and biologicals
were labeled in accordance with currently accepted professional principles for one (200 hall medication
cart) of three medication carts reviewed for medication labeling.
The facility failed to ensure two insulin pens (one Aspart insulin syringe and one Tresiba insulin syringe) on
the 200 hall medication cart had open dates.
The facility failed to ensure two insulin pens on the 200-hall medication cart were discarded 28 days after
being opened. One Lyumjev insulin pen and one Admelog insulin pen had an open date of 1/20/2025 and
was found in the cart on 3/04/2025 (46 days after being opened).
These failures could place residents at risk for not receiving the intended therapeutic effects of prescribed
medication.
Findings included:
In an interview and observation on 3/04/2025 at 8:55 a.m., the 200-hall medication cart contained one
Aspart insulin syringe and one Tresiba insulin pen with no open dates. RN D stated these two insulin pens
were not opened, but the seals were not present on the insulin pens (indicated they were open). The
200-hall medication cart also contained one Lyumjev insulin pen and one Admelog insulin pen that had an
open date of 1/20/2025 (46 days after being opened), and RN D stated these insulin pens were good until
the manufacturer's expiration date because they were long-acting insulins. RN D stated there was no risks
to the residents, and that the nurses using the carts monitored the dates on medications.
In an interview on 3/04/2025 at 9:50 a.m., the DON stated an open date was required for all insulins
including the long-acting insulins. The DON reported insulin should be discarded after 28 days. The DON
reported that not having an open date or using beyond 28 days could cause the medication to not be as
effective. The DON reported the nurses administering medications and the ADONs were responsible for
monitoring the dates on medications. The DON stated her expectation was for all insulins to have an open
date and to be discarded after 28 days.
In an interview on 3/06/2025 at 11:16 a.m., ADON C reported she checked the medication carts for dates
on medications every Tuesday. ADON C stated insulin had to have an open date because it was only good
for 28 days and then must be discarded. ADON C stated if an insulin pen did not have an open date, then it
could not be used and must be discarded. When asked what the risks would be to the residents if insulin
was not dated or used past 28 days, ADON C just stated that insulin could not be used after 28 days, and
staff would not know when the insulin was opened without a date.
Record review of the facility's policy titled Medication Storage, with a date of 1/20/2021, revealed It is the
policy of this facility to ensure all medications housed on our premises will be stored, dated and labeled
according to the manufacturer's recommendations. The policy also revealed medication carts are routinely
inspected for discontinued, outdated, defective, or deteriorated medications with worn, illegible, or missing
labels.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 9 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observations, interviews, and record review the facility failed to store, prepare, distribute, and
serve food in accordance with professional standards for food service safety in the facility's only kitchen
reviewed for food safety.
1.
The facility failed to ensure food items were accurately labeled and dated with the received or expiration
date.
2.
The facility failed to ensure dented cans were placed in a separate storage area.
3.
The facility failed to ensure opened items were sealed or resealed effectively.
These failures could place residents at risk for food-borne illness and cross contamination.
Findings Included:
Observation of dry storage on 03/04/2025 at 9:13am revealed the following:
-1, 1lbs box of cream of wheat dated 02/08/2025 opened and exposed to the air.
- 6 bags of hot dog buns with no use by or expiration date.
-1, 3lbs can of cream of chicken dated 01/08/2027 was dented on bottom left.
In an interview with the DM on 03/04/2025 at 9:30am she stated dented cans were stored in a separate
area in the dry storage closet. She stated when dented cans were identified, she notified the vendor to
receive a credit. She stated when she received bread delivery, the expiration date was printed on the
outside of the package. She stated if the expiration date was not printed on the packaging, she wrote a use
by or expiration date on the packaging. She stated all food items should be properly sealed. She stated
food not stored and labeled properly could cause cross contamination.
In an interview with [NAME] F on 03/05/2025 at 11:19am she stated all food items needed to be sealed
properly and dated with the use by or expiration date. She stated dented cans are stored in a separate area
and returned to the vendor. She stated if items are not sealed, labeled, and stored properly could cause
cross contamination and residents could become sick.
Record review of the facility's Food Storage Policy revised 8/11/ 2017 reflected, Policy Statement: Dry
storage may be in a room or area for the storage of dry goods, such as single service items, canned goods,
and packaged or containerized bulk food that is not PHF/TCS. 6. Products which do not
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675057
If continuation sheet
Page 10 of 11
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
675057
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/06/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Balch Springs Nursing Home
4200 Shepherd LN
Balch Springs, TX 75180
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
FORM CMS-2567 (02/99)
Previous Versions Obsolete
have an imprinted use by or expiration date on the product, will be dated when received and rotated as new
inventory is purchased. 9. All opened products must be resealed effectively and properly labeled, dated and
rotated use. 11. Canned goods that have a compromised seal will be removed from service and stored in a
separate area, until they are picked up by the distributor of discarded.
Record review of the U.S. FDA Food Code 2022 reflected: Chapter 3 . section 3-101.11. Safe,
Unadulterated, and Honestly Presented: . FDA considers food in hermetically sealed containers that are
swelled or leaking to be adulterated and actionable under the Federal Food, Drug, and Cosmetic Act.
Depending on the circumstances, rusted, and pitted or dented cans may also present a serious potential
hazard. Food Labeling [* .(b) A food which is subject to the requirements of section 403(k) of the act shall
bear labeling, even though such food is not in package form. (c The specific artificial color used in a food
shall be identified on the labeling when so required by regulation in part 74 of this chapter to assure safe
conditions of use for the color additive.], 9 CFR 317 Labeling, [*(a) When, in an official establishment, any
inspected and passed product is placed in any receptacle or covering constituting an immediate container,
there shall be affixed to such container a label .Marking Devices, and Containers, and 9 CFR 381 Subpart
N Labeling and Containers, and as specified under § 3-202.18. Section 3-302.12 Food Storage
Containers, Identified with Common Name of Food: Except for containers holding FOOD that can be readily
and unmistakably recognized such as dry pasta, working containers holding food or food ingredients that
are removed from their original packages for use in the food establishment, such as cooking oils, flour,
herbs, potato flakes, salt, spices, and sugar shall be identified with the common name of the food. Section
3-501.17 . Commercial processed food: Open and hold cold . B . 1. The day the original container is opened
in the food establishment shall be counted as Day 1. 2. The day or date marked by the food establishment
may not exceed a manufacturer's use-by date if the manufacturer determined the use-by date based on
food safety . C. 2. Marking the date or day of preparation, with a procedure to discard the food on or before
the last date or day by which the food must be consumed on the premises, sold, or discarded as specified
under (A) of this section. 3. Marking the date or day the original container is opened in a food
establishment, with a procedure to discard the food on or before the last date or day by which the food must
be consumed on the premises, sold, or discarded as specified under (B) of this section. Definitions 3 . Food
Receiving and Storage - Section 3-302.11 Packaged and Unpackaged Food-Separation, Packaging, and
Segregation Food shall be protected from cross contamination by: when combined as ingredients,
separating raw animals' foods during storage, preparation, holding, and display.
Event ID:
Facility ID:
675057
If continuation sheet
Page 11 of 11