F 0584
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to a safe, clean, comfortable and homelike environment, including but not limited
to receiving treatment and supports for daily living safely.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure the resident had a right to a clean and
homelike environment, including but not limited to receiving treatment and supports for daily living safely for
1 of 2 shower rooms and 1 of 15 residents reviewed for environmental concerns. The facility failed to ensure
Hall 400's shower room did not have one shower chair soiled with a brown substance with grayish area
surrounding below the seat. The facility failed to ensure Resident #26's wheelchair and wheelchair cushion
did not have smears of food and food particles.These failures could place residents at risk of a diminished
quality of life due to exposure to an environment that is unpleasant, unsanitary, and unsafe.Findings
include:1. During an observation and interview on 07/06/2025 at 08:45 a.m., Hall 400's shower room had
one shower chair soiled with brown substance with grayish area surrounding below the seat. CNA F and
CNA M acknowledged the soiled areas were below the seat of the shower chair. They said the staff who
provide the daily showers were responsible for cleaning between uses. CNA F said the shower chairs and
shower walls were to be sprayed with a disinfectant spray and rinsed with water after each use. She
acknowledged under the seat of shower chairs had not been cleaned by wiping or using a cleaning brush.
CNA F and CNA M said the disinfectant was kept in a storage cabinet in the shower room and occasionally
had to ask housekeeping for disinfectant.
During an interview on 07/06/2025 at 8:50 a.m., Housekeeper G said the aides were responsible for
cleaning the shower chairs after each use. She said housekeeping was responsible for cleaning the entire
shower area. Housekeeper G said she would also clean shower chairs during her routine if they were
soiled.
During an interview on 07/08/2025 at 2:00 p.m., the DON said her expectations included all shower chairs
to be cleaned between each use. This would include spraying chairs with disinfectant, wiping all surfaces on
top and below before rinsing. The DON said soiled resident equipment could lead to cross-contamination
and potentially cause infections/illnesses due to encountering soiled items.
During an observation and interviews on 07/07/2025 at 09:15 a.m., the shower room for Halls 100/200 was
in use. Both shower chairs were in use during the observation. CNA H and CNA J said the shower chairs
are to be cleaned and disinfected between each resident. CNA H pulled a bottle of disinfectant from storage
cabinet. She said it was to be used on surfaces and chair frames.
During a confidential interview with members of the Resident Council on 07/07/2025 at 10:00 a.m., the
Resident Council said the shower chairs were cleaned between uses with disinfectant and wiped by the
aides, however had not observed shower chairs having been cleaned from underneath the seat.
Record review of Resident #26’s face sheet, dated 07/08/25, indicated a [AGE] year-old male
(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 13
Event ID:
675120
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0584
Level of Harm - Minimal harm
or potential for actual harm
who was admitted to the facility on [DATE]. Resident #26 had diagnoses which included Alzheimer’s
disease and stroke (lack of oxygen to the brain).
Record review of Resident #26’s annual MDS assessment, dated 04/21/25, indicated Resident #26
was with BIMS of 3, which indicated severely impaired cognition. He used a wheelchair daily for mobility.
Residents Affected - Few
Record review of Resident #26's care plan, updated on 07/07/25 after surveyor intervention, indicated
Resident #26 had a behavior problem, resident spits on the wall, floor bed rails and drops food in chairs
and spits food. The goal indicated the resident will have fewer episodes of spitting on the walls, bed, and
floor.
During an observation on 07/06/25 at 11:00 a.m., Resident #26‘s wheelchair and wheelchair
cushion had food particles and food smeared on the sides of the wheelchair, foot pedals and on tires. The
cushion had a beige substance smeared and appeared to be dry and was flaking.
During an interview and observation on 07/7/25 at 12:30 p.m., Resident #26’s family said she never
saw his wheelchair and cushion without food smears and food particles. The wheelchair and cushion had
food smears and food particles. The foot pedals had food particles. She said she had not complained about
the condition of the wheelchair or the cushion to the facility.
During an interview on 07/8/25 at 10:00 a.m., the DON said night shift was responsible for washing
wheelchairs and cushions. Her expectation was for all the wheelchairs to be cleaned each week on the
night shift. She said Resident #26’s wheelchair should have been cleaned on Saturday nights. She
said the wheelchairs being dirty was not homelike and could cause infection control issues.
During an interview on 07/08/25 at 11:00 a.m., the DON said both regular night shift CNAs were on
vacation. She said the charge nurse this past weekend was LVN N and the UM was working on the night
shift and provided direct resident care. She dialed the unnamed night shift CNAs, and we were unable to
leave message.
During an interview on 07/08/25 at 11:30 a.m., LVN N said she was responsible to ensure the CNAs
cleaned the wheelchairs and cushion on the night shift. She said she did not notice Resident #26
wheelchair was dirty.
During an interview on 07/8/25 at 3:15 p.m., the UM said she worked Saturday night (07/05/25) as an aide
but she didn’t recall Resident #26 wheelchair being dirty or if it was washed. She said on the night
shift the wheelchairs were washed weekly.
A facility policy dated May 2017 and titled “Homelike Environment” indicated the following.
…” Residents are provided with a safe, clean, comfortable and homelike environment and
encouraged to use their personal belongings to the extent possible. … 2. The facility staff and
management shall maximize, to the extent possible, the characteristics of the facility that reflect a
personalized, homelike setting. These characteristics include a clean, sanitary and orderly
environment.”
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 2 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0605
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Prevent the use of unnecessary psychotropic medications or use medications that may restrain a resident's
ability to function.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review the facility failed to ensure each resident's drug regimen was free
of unnecessary drugs for 2 of 10 residents (Residents #13 and #34) reviewed for unnecessary medication.
1. The facility failed to monitor Resident #13 for side effects of the antianxiety medication, lorazepam (used
to treat anxiety) routinely and PRN.2. The facility failed to ensure a stop date or reorder date was ordered
for the PRN lorazepam for Resident #13. 3. The facility failed to ensure Resident #13 was monitored for
side effects of the antipsychotic medication quetiapine fumarate (used to treat bipolar disorder).4. The
facility failed to monitor Resident #34 for side effects of the antipsychotic medication Abilify (used to treat
several mental health conditions).These failures could place residents at risk for adverse consequences
and decline in health.Findings include:1. Record review of Resident #13's face sheet, dated 07/06/25,
indicated a [AGE] year-old female who was admitted to the facility on [DATE]. Resident #13 had diagnoses
which included bipolar disorder (disorder associated with episodes of mood swings ranging from
depressive lows to manic highs), dementia (a group of thinking and social symptoms that interfere with
daily function) and anxiety (intense, excessive and persistent worry and fear about everyday
situations).Record review of Resident #13's admission MDS assessment, dated 05/30/25, documented a
BIMS score of 00, which indicated severely impaired cognition. Resident #13 had diagnoses which included
bipolar disorder, depression (a serious mental illness characterized by sadness and a loss of interest in
activities) and anxiety. The assessment indicated Resident #13 received an antipsychotic and antianxiety
medication during the last 7 days.Record review of Resident #13's MAR, dated 07/08/25, indicated
Resident #13 received lorazepam 1 mg at bedtime for dementia and anxiety with a start date of 05/23/25,
Quetiapine fumarate 25 mgs at bedtime for bipolar disorder with a start date of 06/03/25 and lorazepam 1
mg every 4 hours as needed for dementia and anxiety with a start date of 05/23/25 and no stop or reorder
date.Record review of Resident #13's physician orders, dated 07/06/25, indicated Resident #3 was
prescribed lorazepam 1 mg at bedtime for dementia and anxiety with a start date of 05/23/25, lorazepam 1
mg every 4 hours as needed for dementia and anxiety with a start date of 05/23/25 and no stop or reorder
date and quetiapine fumarate 25 mg at bedtime for bipolar disorder with a start date of 06/03/25. The
orders did not address monitoring the antianxiety or antipsychotic medication for side effects or a reorder or
stop date for the PRN antianxiety medication.Record review of Resident #13's care plan, with a target date
of 09/04/25, indicated Resident #13 was prescribed an antianxiety medication with interventions which
included administer antianxiety medication as ordered by physician and monitor, document and report any
adverse reactions every shift and monitor for side effects and effectiveness every shift Resident #13's care
plan indicated she received psychotropic medication with interventions including administer as ordered by
the physician, monitor for side effects and effectiveness every shift. Record review of Resident #13's
electronic medical record, from 05/23/25 to 07/07/25, for Resident #13 did not indicate the nurses'
documented monitoring of side effects of the routine or PRN antianxiety medication lorazepam or the
psychotropic medication quetiapine fumarate with medication administration.During an observation and
interview on 07/06/25 at 9:20 a.m., Resident #13 was sitting on her bed and said she was unsure what
medication she took.2. Record review of Resident #34's face sheet, dated 07/06/25, indicated a [AGE]
year-old female who was admitted to the facility on [DATE] and readmitted on [DATE]. Resident #13 had
diagnoses which included schizoaffective disorder (a combination of symptoms of schizophrenia and mood
disorder such as depression or bipolar disorder) and Alzheimer's disease (a progressive disease that
destroys memory and other important mental
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 3 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0605
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
functions). Record review of Resident #34's quarterly MDS assessment, dated 06/06/25, documented a
BIMS score of 3, which indicated severely impaired cognition. Resident #34 had diagnoses which included
Alzheimer's disease and schizoaffective disorder. The assessment indicated Resident #34 received an
antipsychotic medication during the last 7 days.Record review of Resident #34's MAR, dated 07/08/25,
indicated Resident #34 received Ability 2 mg daily for schizoaffective disorder with a start date of 05/31/25.
Record review of Resident #34's physician orders, dated 07/06/25, indicated Resident #34 was prescribed
Ability 2 mg daily for schizoaffective disorder with an order date of 07/02/25. The orders did not address
monitoring of the antipsychotic medication for side effects.Record review of Resident #34's care plan, with
a target date of 09/07/25, indicated Resident #34 was prescribed a psychotropic medication, Abilify with
interventions including administer as ordered by the physician, monitor for side effects and effectiveness
every shift.Record review of Resident #34's electronic medical record, dated 07/01/25 to 07/07/25, did not
indicate the nurses' documented monitoring of side effects of or the psychotropic medication Abilify with
medication administration.During an observation and interview on 07/06/25 at 8:40 a.m., Resident #34 was
lying in bed and said she was unsure of what medication she took.During an interview on 07/08/25 at 10:00
a.m., LVN C said she was responsible for providing care for Resident #13 and she received lorazepam and
quetiapine fumarate and should be monitored for side effects in the computer system and was not, it was
overlooked. She said she was responsible for providing care for Resident #34 and she received Ability and
should be monitored for side effects in the computer system and was not. LVN C said the nurse ordering
the medication was responsible for adding monitoring into the computer system and the Unit Manager was
the back up. She said she was educated to monitor psychotropic medication for side effects, but it was
overlooked. She said the DON monitored the PRN medication for 14 day stop dates. LVN C said the
resident risk of not monitoring psychotropic medication for side effects was the medication may not be
effective and may not be the correct dose for the resident.During an interview on 07/08/25 at 10:30 a.m.,
the DON said the nurse ordering the medication was responsible for adding side effect monitoring into the
computer system and the UM was the back up to double check and ensure all psychotropic medication was
monitored for side effects. The DON said the nurses were educated on monitoring all psychotropic
medication for side effects. She said these were overlooked. The DON said the resident risk of a
psychotropic medication not monitored for side effects was the resident could have a side effect and staff
be unaware. The DON said she was responsible for adding a 14 day stop date to Resident #13 's PRN
lorazepam and the UM was the back to double check and ensure the stop date was added to the physician
order. She said it was overlooked. The DON said her expectation was all psychotropic medication
monitored for side effects and all PRN psychotropic medication had a 14 day stop date added into the
computer system so they could be reevaluated by the physician as required.During an interview on
07/08/25 at 11:00 a.m., the Administrator said the nurse ordering the medication was responsible for
adding the side effect monitoring into the computer system and the UM was the back up to double check
and ensure all psychotropic medication was monitored for side effects. He said all nurses were educated on
monitoring psychotropic medication for side effects and these were overlooked. The Administrator said the
resident risk of a psychotropic medication not monitored for side effects was the resident could have a side
effect and staff be unaware. He said the DON was responsible for adding a 14 day stop date to Resident
#13 's lorazepam and the UM was a double check. He said the 14-day stop date was overlooked. The
Administrator said his expectation was all psychotropic medication monitored for side effects and all PRN
psychotropic medication had a 14 day stop date added into the computer system so they could be
reevaluated by the physician as recommended.During an interview on
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 4 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0605
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
07/08/25 at 12:45 p.m., the UM said the nurse ordering the medication was responsible for adding the side
effect monitoring into the computer system and she was the back up to double check and ensure all
psychotropic medication was monitored for side effects. She said the DON was responsible for adding a
14-day stop date to PRN psychotropic medication and she was the back up to ensure all PRN psychotropic
medication had a 14 day stop date. She said she did a 24-hour audit on all admissions during the morning
meeting to ensure all orders were put in the computer system correctly and the monitoring for side effects
and 14-day stop date were added to all PRN psychotropic medication. She said she was educated on
monitoring psychotropic medication for side effects and ensuring a 14-day stop date was added to all PRN
psychotropic medication. The UM said they were overlooked. She said the resident risk of was the
possibility of the facility not being aware of an adverse reaction a resident may have.Record review of the
facility's, policy, dated November 2017. titled, Medications indicated, . b. patients must not receive PRN
psychotropic medication orders unless that medication is necessary to treat a diagnoses specific condition
that is documented in the clinical record and are limited to 14-days. If longer than 14-days, the physician
must document their rational in the patient's medical record and are indicate the duration for the PRN order.
c. PRN orders for antipsychotic medications are limited to 14-days and cannot be renewed unless the
physician evaluates the patient for the appropriateness of the medication.8. Behaviors and side effects of
the use of medication must be monitored and documented for Patient/Residents receiving psychotropic
medication.
Event ID:
Facility ID:
675120
If continuation sheet
Page 5 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0645
PASARR screening for Mental disorders or Intellectual Disabilities
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to ensure each resident in a nursing facility was
screened for a mental disorder (MD) or intellectual disability (ID) prior to admission and that individuals
identified with MD or ID were evaluated and receive care and services in the most integrated setting
appropriate to their needs for 1 of 8 residents (Resident #1) reviewed for PASRR screenings. The facility
failed to submit a new PL1 screening to TMHP (a group of contractors that administer Texas Medicaid on
behalf of the Texas Health and Human Services Commission) dated 03/06/25, which indicated Resident #1
had positive evidence of mental illness. This failure could place residents at risk of not receiving specialized
services. Findings include:Record review of Resident #1's face sheet, dated 07/06/25, indicated a [AGE]
year-old-female who was admitted to the facility on [DATE] and readmitted [DATE]. Resident #1 had
diagnoses of generalized anxiety disorder (severe, ongoing anxiety that interferes with daily activities) and
major depressive disorder (a serious mental illness characterized by persistent sadness, loss of interest in
activities and symptoms that interfere with daily life).Record review of Resident #1's PASRR Level 1
Screening, dated 09/29/23, indicated Resident #1 was negative for mental illness, intellectual disability, and
developmental disability and negative for dementia as the primary diagnosis. Record review of Resident
#1's PASRR Level 1 Screening, dated 03/06/25, indicated Resident #1 was positive for mental illness,
negative for intellectual disability, and developmental disability and negative for dementia as the primary
diagnosis. There was no PASRR Level II Screening or Form 1012 (Mental Illness/Dementia Resident
Review) found in the clinical record from the resident's admission on [DATE] through 07/07/25.Record
review of Resident #1's care plan, initiated on 05/02/25 indicated, Resident #1 received psychotropic
medication for depression of bupropion with a goal to monitor and report adverse reactions. Record review
of Resident #1's most recent significant change MDS assessment, dated 06/21/25, indicated Resident #1
was not PASRR positive and had a BIMS score of 7, which indicated severely impaired of cognition.
Resident #1 had diagnoses which included major depressive disorder and anxiety.Record review of
Resident #1's physician orders, dated 07/18/25, indicated she was prescribed bupropion HCL 150 mgs XL
(antidepressant medication) every day for major depressive disorder with a start date of 04/01/25. During
an observation and interview on 07/06/25 at 9:48 a.m., Resident #1 was lying in bed and said she was
treated well and received needed care and services. During an interview on 07/07/25 at 11:29 a.m., the
MDS Nurse said she was responsible for all PASRR forms in the facility and was educated on PASRR
completion. She said her back up was the Regional MDS Coordinator. The MDS Nurse said Resident #1
was considered PASRR negative but had a PL1 dated 03/06/25 which indicated she was positive for mental
illness uploaded into the facility's computer system but not sent into TMHP through Simple LTC (long term
care software that facilitates claims data analysis and regulatory compliance, reimbursement optimization
and quality measurement for healthcare practices). She said she would send in a 1012 form (Mental Illness/
dementia resident review- form used to determine if a resident initially assessed as not needing further
evaluation for Mental illness or dementia requires a more in-depth assessment based on new information or
changes in their condition) and new positive PL1 immediately. She said the PL1 was overlooked and should
have been sent into TMHP on admission. The MDS Nurse said the resident risk of a resident's positive PL1
not sent into TMHP was a resident's needs may not be met. She said the positive PL1 was overlooked
before she was hired on 04/01/25.During an interview on 07/08/25 at 10:30 a.m., the DON said the MDS
Nurse was responsible for all PASSR forms in the facility and was educated on correctly completing PASRR
forms. She said the Regional MDS Coordinator was the back up. The DON said Resident #1's PL1 form
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 6 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0645
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
was overlooked and only uploaded into the facility's computer system and not uploaded into the Medicaid
system. She said the resident risk was a potential lack of services for the resident. The DON said her
expectation was every resident had a PL1 form completed on admission and uploaded into the Medicaid
system and if it was positive for the resident to receive needed services. During an interview on 07/08/25 at
11:00 a.m., the Administrator said the MDS Nurse was responsible for all PASSR forms in the facility and
the Regional MDS Coordinator was the back up. He said the MDS Nurse was educated on completion of
PASRR forms and Resident #1's PL1 form was overlooked and only uploaded into the facility's computer
system and not uploaded into the Medicaid system. The Administrator said the resident risk was a potential
lack of services. The Administrator said his expectation was every resident had a PL1 form completed on
admission and uploaded into the Medicaid system and if it was positive for the resident to receive needed
services. During an interview on 07/08/25 at 4:17 p.m., the Regional MDS Coordinator said the MDS Nurse
was responsible for all PASSR forms in the facility, and she was the back up. She said she spot checked
MDSs and PASRR forms and would cover the facility if the MDS Nurse was out on leave. The Regional
MDS Coordinator said the MDS Nurse was educated on completion of PASRR forms. She said Resident
#1's PL1 form was overlooked and only uploaded into the facility's computer system and not uploaded into
the Medicaid system. She said the resident risk was a resident may not receive PASRR services she
should be receiving.Record review of the October 2023 Long-Term Care Facility Resident Assessment
Instrument 3.0 User's Manual titled, A1500: Preadmission Screening and Resident Review (PASRR) Item
Rationale Health-related Quality of Life indicated . o All individuals who are admitted to a Medicaid certified
nursing facility, regardless of the individual's payment source, must have a Level I PASRR completed to
screen for possible mental illness (MI), intellectual disability (ID), developmental disability (DD), or related
conditions . o Individuals who have or are suspected to have MI or ID/DD or related conditions may not be
admitted to a Medicaid-certified nursing facility unless approved through Level II PASRR determination.
Those residents covered by Level II PASRR process may require certain care and services provided by the
nursing home, and/or specialized services provided by the State Record review of the facility's, undated,
policy titled PASRR Process indicated, PASRR is required of each state's Medicaid program to ensure that
those with Mental Illness (MI)/ Intellectual or Developmental Disability (IDD) are cared for properly . PCC submits the PL1 and becomes the gate keeper of all things PASRR.
Event ID:
Facility ID:
675120
If continuation sheet
Page 7 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review the facility failed to ensure that the medication error rate was less
than five percent or greater. The facility had a medication error rate of 7.79% based on 2 errors out of 26
opportunities, which involved 2 of 6 residents (Residents #6 and #49) and 2 of 3 staff observed during
medication administration reviewed for medication error. 1. The facility failed to ensure LVN A administered
Dorzolamide Solution 2% Ophthalmic (eye drops) per facility policy to Resident #49. 2. The facility failed to
ensure LVN B did not administer Levothyroxine 75 MCG to Resident #6 on an empty stomach. These
failures could place residents at risk of unwanted side effects and not receiving the therapeutic dosage of
medications.
Residents Affected - Few
Findings include:
1. Record review of Resident #49's face sheet indicated a [AGE] year-old male who was admitted to the
facility on [DATE]. His diagnoses included rhabdomyolysis (a breakdown of muscle tissue that releases a
damaging protein into the blood), and open-angle glaucoma (a chronic eye condition where the
eye’s drainage canals gradually clog, leading to a slow increase in the intraocular pressure).
Record review of Resident #49's Quarterly MDS assessment, dated 04/18/25 indicated a BIMS score of 10,
which indicated Resident #49's cognition was moderately impaired.
Record Review of Resident #49's physician orders dated July 2025 indicated Dorzolamide Ophthalmic
Solution 2% instill 1 drop each eye two times daily for glaucoma.
Record review of Resident #49's medication administration record (MAR) dated 07/08/25 indicated
Dorzolamide ophthalmic solution 2% instill one drop in both eyes two times a day for Glaucoma at 7:00
a.m. and 7:00 p.m.
During an observation of medication pass on 07/07/25 at 7:18 a.m., LVN A instilled Dorzolamide ophthalmic
solution 2% one drop into the inner corners of each eye.
During an interview on 07/08/25 at 11:14 a.m., LVN A said she always administered eye drops to the inner
corners of the eyes and was careful not to place the drop directly on the eyeball. She said Resident #49
usually pulled his own lower lid down, but he had not done so today. She said even on days when he did
pull his lower eye lid down, she still administered his eye drops into the inner corners of his eyes. She said
she did not know what facility policy said about administering eye drops. She said the facility watched her
give medications including eye drops and had never instructed her she should administer the drops
differently.
2. Record review of Resident #6's face sheet indicated a [AGE] year-old male who was admitted to the
facility on [DATE]. His diagnoses included Parkinsonism (a syndrome characterized by tremor, bradykinesia
(slowness of movement) , rigidity, and postural instability) and dementia (a group of thinking and social
symptoms that interferes with daily functioning).
Record review of Resident #71 's quarterly MDS assessment dated [DATE] indicated a BIMS score of 4,
which indicated Resident #6’s cognition was severely impaired.
Record review of Resident #6's physician orders dated July 2025 indicated Levothyroxine Sodium 75
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 8 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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
MCG give one tablet by mouth one time a day for low thyroid hormone.
Level of Harm - Minimal harm
or potential for actual harm
Record review of Resident #6's MAR dated 07/08/25 indicated Levothyroxine Sodium 75 MCG give one
tablet by mouth one time a day for low thyroid hormone at 8:00 a.m.
Residents Affected - Few
During a medication pass observation and interview on 07/08/25 at 8:05 a.m., LVN B administered the
following medications to Resident #6 orally:
- Benztropine 1mg 1 tablet
- Famotidine 20mg 1 tablet
- Iron 325mg 1 tablet
- Haloperidol 1mg 1 tablet
- Levothyroxine Sodium 75MCG 1 tablet
- Oxcarbazepine 200mg 1 tablet
- Paliperidone ER 3mg 1 tablet
- Vitamin D 325MCG 1 tablet
- Clonazepam 1mg 1 tablet
LVN B said Resident #6 had just finished his breakfast.
During an interview on 07/08/25 at 11:55 a.m., LVN B said Levothyroxine should always be given on an
empty stomach for best absorption. She said she usually gave Resident #6’s medications before
breakfast, but she had been running late and gave all his medications after he had eaten. She said giving
the Levothyroxine with breakfast and other medications could interfere with the medication's absorption and
it might not be as effective.
During an interview on 07/08/25 at 3:05 p.m., the DON said the facility policy was to instill eye drops by
averting the lower lid and instilling the drop into the pocket created by averting the lower eye lid. She said
the Pharmacy Consultant for the facility watched medication pass with the nurses quarterly. She said she
had called the Pharmacy Consultant, and she said she was surprised because she had observed LVN A
administering eye drops by averting the resident's lower eye lid and instilling the drop into the pocket. She
said that when the facility changed to the electronic medical record (EMR) systems on April 1st, 2025, all
thyroid medications had been rescheduled to be given at 8:00 a.m. She said the former EMR system had
all thyroid medications scheduled to be given at 6:00 a.m. She said she reviewed all resident's records and
corrected the scheduling error for all thyroid medications. She said he was the direct supervisor of all
nursing staff. She said she expected all medications to be given according to facility policy, medication
recommendations, physician orders, and the 6 rights of medication administration. She said the possible
negative outcome of administering eye drops into the inner corners of the eyes and thyroid medications
with other medications on a full stomach was decreased absorption of the medications.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 9 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Record review of the facility’s undated policy titled Medication Administration indicated … *Use
index or middle finger to pull down the eye lid and instill drop into lower lid conjunctival sac. You can no
longer drop onto the eyeball” …
Record review of Synthroid.com indicated … “The way you take Synthroid (Levothyroxine) can
affect how much your body is getting. … Take Synthroid once a day, every day at the same time before
breakfast. Only take Synthroid with water and on an empty stomach. Wait 30 minutes to 1 hour before
eating or drinking anything other than water.” …
Event ID:
Facility ID:
675120
If continuation sheet
Page 10 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0813
Have a policy regarding use and storage of foods brought to residents by family and other visitors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to maintain and ensure safe and sanitary
storage of residents' food items for 1 of 1 residents room reviewed for food safety (room [ROOM NUMBER])
in that: The refrigerator located in room [ROOM NUMBER] was not monitored for expiration/used by dates.
This failure could place residents at risk for food illnesses. Findings included:During an observation and
interview on 07/06/2025 at 09:30 a.m., revealed the following expired items in Resident #2's personal
refrigerator:-one 18-ounce bottle of mayonnaise with expiration date of 06/16/2025;- one 9-ounce package
of ham lunch meat with expiration date of 07/02/2025;-one 15-ounce bottle of sandwich spread with
expiration date of 12/02/2024;-one 13 -ounce bottled cold coffee drink with expiration date of
02/03/2025;-two 8-ounce supplemental milk shake with expiration date of 02/01/2025;-one 15-ounce bottle
of mayonnaise with expiration date of 06/11/2025; and-one 20-ounce strawberry Jell-O with expiration date
of 04/04/2024. Resident #2 said her family brought her the items. She said the nursing staff would hand her
whatever items she requested. Resident #2 said she did not know who was responsible to oversee items in
the refrigerator for expiration dates. The Regional Clinical Director of Services was present and disposed of
the expired items. She said they should not have remained available after the expiration date on each item.
Consumption could lead to food-borne illnesses. During an interview on 0708/2025 at 2:00 p.m., the DON
said nursing staff were expected to check items for expirations weekly. She said all food from outside
should be dated when opened and discard when reached expiration date. Consumption of expired food or
drink could cause negative adverse effects including gastrointestinal symptoms. Record review of the
facility policy, dated November 2016, and titled Patient/Resident Food from Outside indicated the
following:1) Patients/Residents may accept food from family and visitors as part of their foodchoices.2) The
facility staff should monitor foods being brought to Patients/Residents to ensurethe food items do not place
the Patient/Resident at risk for choking based upon anyphysician ordered restrictions.3) Food or beverages
brought in from the outside will be dated. Food items placed [NAME] common refrigerator/freezer will also
be labeled with the patient's/resident's nameand room number.4) The facility staff should monitor and assist
Patients/Residents and visitors with safefood handling practices to ensure avoidance of food borne
illnesses.5) Food or beverages in the original container that is past the manufacturer's expirationdate will be
discarded by the facility staff.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 11 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0925
Make sure there is a pest control program to prevent/deal with mice, insects, or other pests.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review, the facility failed to maintain an effective pest control
program for 1of 1 kitchens reviewed for effective pest control in that: Numerous flies were observed
throughout the kitchen during the noon meal preparation time on 07/07/2025. This failure could place
residents at risk for spread of infection, cross-contamination, and decreased quality of life.Findings
included: During observations and interviews on 07/07/2025 from 11:00 - 12:00 noon, during meal
preparation and serving, numerous flies were swarming throughout the preparation area. Flies were
observed landing on steamtable, cabinets, near handwashing sink, and near food cart. Six or 7 flies were
killed with flyswatter within this period. [NAME] D and dietary aide E acknowledged the numerous flies and
said the flies would come in through the side exit door of the kitchen which was approximately 10 yards
from the rear exit door to the facility. They added the flies seemed to come inside more after it had rained.
They said facility staff were constantly going in and out of the back door because it would lead to the
laundry area, parking lot, and the garbage dumpster. During an interview on 07/07/2025 at 09:45 a.m., the
DM (dietary manager) said she had been aware of flies in the kitchen area. She said she had requested the
kitchen staff not use the side exit door from kitchen due to it being near the rear exit door of facility. She
said she had requested the facility to obtain a fly trap wall sconce for the kitchen. She said a potential
negative outcome would be cross contamination of food, possibly causing food-borne illnesses. She said
should an insect land on the food, it would have to be thrown out and possibly delay meals for the
residents. During a confidential interview with members of the Resident Council on 07/07/2025 at 10:00
a.m., the Resident Council said they had observed numerous flies in dining room on occasion. They said
they sometimes would swat flies at mealtimes. Resident Council members said obviously the facility pest
control was ineffective. During observations and interview on 07/08/2025 at 08:00 a.m., the maintenance
supervisor acknowledged the facility had concerns with flies outside the rear exit of facility which also led to
side entrance door to kitchen. He said there were 3 fly trap light wall sconces throughout facility.
Observations were made of the 3 fly trap wall sconces with these results:#1 located at rear exit door - the
sticky strip was missing;#2 located in closed hallway leading from Hall 400 to exit door near laundry; and #3
located in common area in front lobby of facility - the sticky strip was missing.The maintenance supervisor
said without the sticky strip in the wall sconces, the flies were less likely to be trapped and eliminated. He
said the facility had a pest control service that would come to facility monthly. He said he was responsible
for ensuring sticky strips were intact as well. Record review of the facility contracts revealed a contract,
undated, for pest control service was in place. Record review of the pest control visit logs indicated the pest
control service visited the facility monthly with last visit 06/25/2025.During an interview on 07/08/2025 at
8:30 a.m., the Administrator said the pest control service came out monthly to service the fly trap sconces.
He said the most recent service was 06/25/2025 and at that time he had requested a 4th sconce to be
delivered. The administrator said the fly trap sconces work by ultraviolent light and sticky pads that were
designed to trap any insect that flies and lands on the strip including flies, bugs, wasps, etc. During an
interview on 07/08/2025 at 2:00 p.m., the DON said her expectations were for there to no flying insects or
rodents in the kitchen or dining area. She said the facility had fly traps located in specific areas. She said a
negative outcome would be flies or insects getting into resident food. She said it would be unsanitary, cross
contamination, and could potentially cause symptoms related to stomach issues. Record review of facility
policy dated May 2008 titled Pest Control indicated facility shall maintain an effective pest control policy. 1.
This facility maintains an on-going pest control
Residents Affected - Some
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 12 of 13
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
675120
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/08/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Woodville Health and Rehabilitation Center
102 N Beech St
Woodville, TX 75979
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 0925
program to ensure that the building is kept free of insects and rodents. 6. Maintenance services assist,
when appropriate and necessary, in providing pest control services.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675120
If continuation sheet
Page 13 of 13