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.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to maintain medical records that were complete, accurate,
readily accessible, and systematically organized for 1 (Resident #11) of 24 residents reviewed for Advance
Directives.
The facility failed to have complete, accurate and readily accessible records to identify Resident #11's code
status. Resident #11's medical record indicated Resident #11 code status was DNR, but the OOH-DNR
form was not in Resident #11's medical record.
This failure could affect residents who have implemented Advance Directives and established their choice
to not be resuscitated at risk of receiving CPR against their wishes.
The findings were:
Record review of Resident #11's Physician's Orders dated [DATE] indicated Resident #11 was a 90-year
female admitted to the facility on [DATE] with diagnoses of Essential Hypertension, Non-ST elevation
myocardial infarction (a type of heart attack that usually happens when your heart's need for oxygen can't
be met), dementia, mild, without behavioral disturbance, psychotic disturbance, mood disturbance (an early
stage of memory loss), and chronic kidney disease, stage 3A (mild to moderate loss of kidney function).
Record review of Resident #11's annual MDS assessment dated [DATE] indicated Resident #11 was
understood by others, understood others, had good memory recall and had the cognitive skills for making
decisions daily.
Record review of Resident #11's care plan dated [DATE] revealed Resident #11 had code status of DNR
with interventions that included, if resident is unresponsive, check for pulse, b/p, and respirations, if resident
is unresponsive notify licensed staff immediately, review wishes annually and/or appointed healthcare
representative.
Record review of Resident #11's Physician's Orders dated [DATE] revealed Resident #11 had an order for
DNR-Do Not Resuscitate dated [DATE].
Record review of Resident #11's electronic record did not reveal an OOH-DNR form.
In an interview on [DATE] at 12:43 PM, the FM of Resident #11 said Resident #11 is a DNR. The FM said
Resident #11 has told me several times that she does not want to be revived or put on a machine.
(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:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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
The FM said the SW called her today to ask her to come to the facility so she could sign the DNR form. The
FM said she thought Resident #11 already had a DNR form when she came from the hospital. FM said
maybe the form wasn't valid, so they asked her to come to the facility and sign another DNR form. The FM
said she had come in and signed the form.
In an interview on [DATE] at 3:17 PM, ADON/LVN E said she checked PCC for Resident #11's record for
the code status and it said Resident #11 code status was DNR. ADON/LVN said she asked the Medical
Records clerk why Resident #11 was a DNR if they could not find any form to indicate she was a DNR.
ADON/LVN E called the family and the FM said she had signed the DNR form. THE ADON/LVN E asked
where she had signed the form and the FM said at the hospital. ADON/LVN E told the FM that the form was
valid only at the hospital and the facility needed an OOH-DNR. The FM came in to sign the DNR form on
[DATE], and the doctor was at the facility, so the form was signed by both.
In an interview on [DATE] at 2:21 PM RN D said if a resident comes from the hospital the resident would be
asked on admission if they were full code or DNR. If the resident was a DNR and something happened to
the Resident, but they do not have the DNR form, and they do not resuscitate, the family could come in and
say the resident was full code. If the resident was being admitted and the resident said they wanted to be
DNR status, then the facility would start working on the DNR form right away.
In an interview on [DATE] at 2:40 PM The SW said she did not fill out the DNR forms. The BOM assistant
was the one that filled out the forms. The SW said she would only fill out the form if a family member came
in and asked for her assistance. The SW said she did not audit the DNR forms to check if they were filled
out correctly because she did not fill them out. The Medical records clerk takes the forms to the doctor to
sign and then he would upload the form to PCC.
In an interview on [DATE] at 8:57 AM, BOM Assistant said she did not fill out the DNR forms, the SW would
fill out the DNR forms. The BOM Assistant said she would let the SW know the new admitting resident's
code status was a DNR, so the SW could start the process. The BOM Assistant said she conducted the
admission process and would check on PCC for the code status and if the resident code status was DNR,
she would then follow up with the family or the resident if they were a DNR. The BOM Assistant would then
let the SW know so the SW could get the form signed by all the necessary parties. Then the Medical
Records Clerk would put the Advance directive in PCC.
In an interview on [DATE] at 9:03 AM, Medical Records Clerk said when a resident comes from the
hospital, sometimes they would come in with a DNR code status and during the meeting the staff would ask
if the resident still wanted the DNR code status. If the resident did want to continue with the DNR code
status, the SW was informed, and she assisted the family or resident with completing the form. Once the
form was signed by the resident or representative, the SW would give the form to the Medical Records
clerk. The Medical Records Clerk said he would send the form by carrier for the doctor's signature or if the
physician comes to the facility, he can sign it here. Once the form was signed, the Medical Records Clerk
would scan the form and send a copy to each department. Then it was up to each department to do their
part.
In an interview on [DATE] at 9:14 AM, MDS/LVN F said if a resident's code status was DNR, the resident
would have an order from the physician and an OOH_DNR form. The staff would verify with the
family/resident that the resident's code status was a DNR. The SW would assist the family with completing
the form. Once the form was signed by all necessary persons the form would be uploaded to PCC. Then
MDS would look for the order and would look under the miscellaneous tab in PCC for the form and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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
then the care plan would be developed. MDS/LVN said she did not know how the care plan was developed
for Resident #11 if they did not have the form.
In an interview on [DATE] at 9:21 AM, the DON said Resident #11 came in from another nursing home as
DNR. The SW would meet with the family and will initiate the process for the DNR. The SW would get it
filled out and then the form goes to medical records. Medical Records Clerk would make sure it had all
signatures and would upload to the form onto PCC and let all nursing departments know that Resident was
now DNR. The MDS department will develop the care plan and will also check for the DNR form. The DON
said she did not know how the error occurred. If Resident #11 had coded, they would still call the resident's
loved one. The DON said sometimes the family would change their minds. The DON said if they started
performing CPR once they start, they cannot stop. The DON said the DNR form might have been deleted
from PCC by mistake. The DON said she would call the IT department and ask if the form was in PCC and
if it could be retrieved.
In an interview on [DATE] at 9:39 AM The SW said she would look at the referrals from the hospital and
checked if they were full code or DNR status, but she did not review the DNR forms to check if they were
correctly filled out or check if they were in the chart. The SW said the Medical Records Clerk would take the
forms to the doctor to be signed and then would make sure the form had all the signatures and would scan
the form and upload it onto PCC.
In an interview on [DATE] at 11:09 AM, The Administrator said the SW was responsible for making sure the
DNR form was in place and during care plans would review the code status and would review the form at
that time. The Administrator said Resident #11 came in as a DNR from the hospital so there should be a
DNR form somewhere. The Administrator said they had a couple of boxes with old medical records so they
would go through them to look for the DNR form.
In an interview on [DATE] at 12:31 PM, the DON provided the hard copy of the DNR form dated [DATE].
The DON said they had looked through boxes of old medical records and found Resident 11s DNR form.
Record review of facility's policy on Advance Directives and Associated Documentation dated 11/2016 and
revised on 12/2023 revealed:
Procedure:
5. When an Advance Directive is completed:
a. Review the Advance Directive to validate the document reflects the resident's choices and that the
document is signed and dated by the resident or responsible agent.
6. Obtain a copy of the Advance Directive ad conservatorship/guardianship documents and place in
resident's health record.
b. Once the advance directive or information regarding resident preferences regarding treatment options is
received by the facility, it will be confirmed in the resident medical record and communicated to members of
the care plan team.
c. The facility will notify the attending physician of advance directives so that, if necessary, appropriate
orders can be documented in the resident's medical record and plan of care.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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
i. A No CPR or DNR telephone order may be used once the Advance Directivee documents are received
and in the health record.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Provide and implement an infection prevention and control program.
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 establish and maintain an infection prevention
and control program designed to provide a safe, sanitary, and comfortable environment and to help prevent
the development and transmission of communicable diseases and infections for two (Resident #78 and
Resident #241) of five residents reviewed for infection control in that:
Residents Affected - Few
1. LVN A failed to properly disinfect equipment after providing wound care for Resident #78.
2. LVN A failed to wear appropriate PPE while providing device care for Resident #241.
3. LVN A failed to change all required items during device dressing care for Resident #241.
These deficient practices could place residents at risk of infection, transmission of communicable diseases,
and a decline in health.
The findings included:
1. Record review of Resident #78's admission record revealed a [AGE] year-old female admitted to the
facility on [DATE]. Diagnoses included encounter for orthopedic aftercare following surgical amputation,
other acute osteomyelitis (infection of the bone) of right ankle and foot, acquired absence of right toe(s),
sepsis (life threatening complication of an infection), pneumonia (infection of the lungs), and need for
assistance with personal care.
Record review of Resident #78's admission MDS dated [DATE] revealed Resident #78 had a BIMS score of
15 which indicated that she was cognitively intact.
Record review of Resident #78's physician order summary report on 05/07/24 revealed an order that read,
Cleanse right foot with NS (normal saline), pat dry with gauze, apply Medi honey, cover with gauze and
wrap with kerlix (woven gauze used to cushion and protect wounds) daily every day shift for surgical post of
amputation and enhanced barrier precautions: wound, every shift.
Observation of Resident #78's wound care on 05/07/24 at 08:51 am, done by LVN A and assisted by LCNA
revealed that LVN A used a pair of bandage scissors to cut the dressing off of Resident #78's right foot.
When wound care was completed, LVN A took the bandage scissors back out into the hallway to the wound
cart. LVN A unlocked and opened the wound cart and got an alcohol prep (approximately 1 inch by 1 inch 2
ply non-woven pad that contained 70% isopropyl (rubbing) alcohol), out and wiped only the scissor blades
with it. LVN A then placed the scissors back into the left side of the top drawer of the wound care cart. LVN
A then wiped down the table and hand sanitizer bottle with disinfectant wipes. The disinfectant wipes
contained isopropyl alcohol and quaternary ammonium (a type of chemical used to kill bacteria, viruses
and mold).
In an interview on 05/07/24 at 09:44 am, LVN A stated it was very important to wipe down equipment and
that she used alcohol on the scissor blades because she thought it was a 100% clean. LVN A stated if
equipment was not wiped down with disinfectant wipes, it could lead to cross contamination which could
lead to infection for the next resident it was used on. That could lead to sepsis, hospitalization, or death for
the resident.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
In an interview on 05/07/24 at 2:47 pm, the DON stated that equipment was wiped with disinfectant wipes
to prevent the spread of infections and if equipment was not cleaned/disinfected, it could cause cross
contamination which could lead to multiple organism growths and hospitalization for other residents.
In an interview on 05/08/24 at 01:14 pm, the ADON stated, No, we should not use alcohol preps to clean
any equipment. We were always supposed to use disinfectant wipes to clean equipment/ supplies/ surfaces.
If not done correctly, it could cause cross contamination, infections, and could lead to an outbreak, facility
acquired infections or hospitalizations.
Record review of the facility's Infection Prevention and Control Program dated 06/2021 and
revised/reviewed 10/2022 stated in part:
Goals:
-Decrease the risk of infection to residents and personnel.
-Recognize infection control practices while providing care.
-Identify and correct problems relating to infection control.
-Ensure compliance with state and federal regulations related to infection control.
-The facility will provide areas, equipment, and supplies to implement its Infection Control Program with the
goal of:
-Effective cleaning and disinfecting equipment as needed.
-Chemicals and equipment used for cleaning and disinfecting will be used in accordance with
manufacturer's directions and recommendations.
2. Record review of Resident #241's admission record revealed a [AGE] year-old female admitted to the
facility on [DATE]. Diagnoses included sepsis (life threatening complication of an infection), unspecified
staphylococcus (bacteria that cause skin infection) as the cause of diseases elsewhere classified,
cutaneous abscess (localized collection of pus in the skin) of right foot, type 2 diabetes, and need for
assistance with personal care. Resident #241 had no known allergies.
Record review of Resident #241's admission MDS dated [DATE] revealed Resident #241 had a BIMS score
of 11 which indicated she had some cognitive impairment but was able to make her needs known and was
oriented to self, place, and situation.
Record review of Resident #241's physician order summary on 05/08/2024 revealed an order that read,
Enhanced Barrier Precautions: PICC line- every shift and PICC LINE CARE: CHANGE PICC LINE
DRESSING Q 7 DAYS IF SITE IS VISIBLE FOR ASSESSMENT. CHANGE DRESSING PRN IF WET,
SOILED,
SATURATED OR LOOSE. every day shift every Sun.
Record review of Resident #241's progress notes reveal an entry created by LVN A on 05/09/24 at 11:18
am with an effective date of 05/08/24 at 3:16 pm, that read, Note Text: picc line dressing
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
changed to rua,dressing [sic] noted with tape dislodging. sterile technique applied, pt tolerated well. pt and
spouse aware. (PICC line dressing changed to right upper arm .)
Observation on 05/08/24 at 2:21 pm with LVN A of Resident #241's entry way revealed an enhanced barrier
precautions sign posted next to the door. Observation of Resident #241's PICC (a thin, long, soft catheter
that is inserted into a vein of the upper arm and ending in a large vein that carries blood into the heart; used
for long term intravenous antibiotics) line dressing revealed she had a right upper arm PICC line that had a
folded piece of gauze under the clear dressing and a stat lock (a stabilization device used to hold the
catheter in place) underneath the transparent dressing. There was tape on the entire right side of the
dressing, indicating that the right side of the original dressing had come loose and had been taped back
down. The tape was not adhered to the skin. LVN A stated the dressing needed to be changed because it
was coming up on one side.
Observation on 05/08/24 of the PICC line dressing change for Resident #241 performed by LVN A revealed
that LVN A failed to put on a gown prior to or during the dressing change, as per the Enhanced Barrier
Precautions sign outside the resident's door. It was noted that the central line dressing kit did not have a bio
patch (an absorptive foam disc that is impregnated with chlorhexidine placed on top of the PICC line
insertion site to aid in preventing blood stream infections) in it. LVN A stated, The bio patches usually come
from the hospital. That I know of, we don't have them. We just put the split gauze on it. LVN A did not take
the stat lock off the catheter or replace the two saline/heparin locks (needleless connectors used to seal off
the IV catheter at the end where the medication is injected). LVN A did not clean the skin around the
insertion site with the three PVP (Povidone Iodine) swab sticks or the three alcohol swab sticks provided in
the kit. LVN A used the alcohol swab sticks to wipe down only the exposed PICC line catheter. The skin
area around the insertion site that would be covered by the dressing was not cleaned. LVN A also did not
use the skin protectant swab (used to help reduce the possibility of irritation from the adhesive in the
transparent dressing) that was provided in the kit to provide a barrier film under the dressing. The PICC line
was sutured into place, so LVN A was unable to slide a split gauze under it at the insertion site. Instead,
LVN A unfolded the split gauze completely and laid it over the top of the entire external part of the PICC
line, then placed the transparent dressing over it.
In an interview on 05/09/24 09:49 am, with the DON and the CRN, the DON stated if the dressing has
gauze under it, it should be changed every 7 days. The CRN stated, that's what our policy states. In
reference to the PICC line having a stat lock, the DON stated, it didn't say a time frame in the policy. The
CRN added, I don't think it says a date or anything. it's just best judgement. The DON stated if dressings
aren't changed frequently enough or if they become soiled or loose, it could get infected, which could lead
to sepsis. The CRN added, it could lead to catheter associated infection. When asked whether the facility
carried stat locks the CRN stated, we have to go check supplies to see if we have the IV stat locks and the
saline/ heparin locks.
The CRN stated that Enhanced Barrier Precautions has been ongoing training, they've been talking to staff
about it ever since it came out. The CRN further stated, If we are not doing formal training, we are out there
talking to them and reminding them. We started training on it in Feb and March and it has been ongoing
ever since. The DON and CRN both stated that Enhanced Barrier Precautions applied to anyone with a
medical appliance or wound and that staff were to wear a gown whenever they touched the device or
provided care.
Observation in the med storage room with the DON and CRN on 05/09/24 at 10:02 am revealed there were
saline/ heparin locks present in a bag hanging on the peg board. The CRN stated, I'm not sure how
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
often they're changed, I'll have to check the policy on that.
Level of Harm - Minimal harm
or potential for actual harm
In an interview on 05/09/24 at 10:07 am, the ADON stated, PICC line dressings are changed every week
and as needed if it becomes loose, wet, soiled, or peeling on the edges. If there was gauze under it, it is
every 3 days, but I'll have to check the policy. The ADON further stated, If there was a stat lock in use, it
gets changed with the dressing change. I have never seen stat locks here. Our kits do not have them. If
there is a stat lock on there, it needs to come off when the dressing is changed, even though we don't have
them. The connectors (saline/heparin locks) are changed weekly and as needed. IV tubing is changed
every 24hours. To keep the end clean, the nurses put an alcohol impregnated cap on it. There are alcohol
caps for the connectors (saline/ heparin locks), also. If the dressing is being changed, everything gets
changed. All the nurses are sent for their IV validation- it is a half day course and is done by an RN that
works for the parent company. The ADON stated the facility always has monthly education with the parent
company nurse and that the new nurses went to IV training a couple of weeks ago. The ADON stated the
nurses should know to change the dressing on a PICC/central/midline if it is loose, soiled, etc. In reference
to IV medication, the ADON stated, If someone is getting any IV medication every 12 hours, the empty bag
and tubing stay in the room until the next use. Then after 24 hours, it is all thrown out and new tubing it
used. The ADON explained Enhanced Barrier Precautions were required when staff was doing wound care,
incontinent care, transferring, oral care- any direct contact with a resident. The ADON explained the
purpose of EBP was to prevent spreading infections from one resident to another and it was used on any
resident that has a device, MDROs (multiple drug resistant organisms), foleys, nephrostomy tubes (a small
flexible tube that goes from an opening in the back into the kidney and is used to drain urine from the
kidney to a urine collection bag), etc. and used for dressing changes on lines, foley care, and dressing
changes on wounds. The ADON stated the facility had just implemented it in March. The facility did a formal
in-service in March, and it has been ongoing and daily. The ADON stated, every day I round and check new
admissions. If they have lines, foleys, wounds, etc., I let the staff know, place the sign at the door and make
sure the gowns are accessible. The gowns are placed in the room in a drawer with a little gown picture on it.
Once staff finished with the gowns, they are thrown in the trash. The trash bag was tied and taken to the big
bin that goes to the outside trash.
Residents Affected - Few
In an interview on 05/09/24 at 10:29 am, LVN A stated, PICC dressings are changed every 7 days or when
needed and can be changed by any qualified nurse. If there was gauze used with the dressing, I would
change it every 4 to 7 days. If there was a stat lock on it and it was not loose or soiled, I would leave it on. In
7 days, I would just take it off because we do not have them in this facility. The connectors are changed
every 7 days. If I was changing the dressing before 7 days, I would change the connectors, also. IV tubing is
changed every 24 hours. If a resident had every 8 or every 12-hour infusions, cover the bag and tubing,
after the date is checked, and put an alcohol impregnated protector on the end of it in between uses.
LVN A also stated, EBP was used to prevent infection. We used EBP whenever the resident had something
that was open. If there was a sign on the door it meant the resident had a device, wound or infection. EBP
meant staff was supposed to use gloves and gown for wound care, peg tube care or use, IVs and anything
that required touching the resident.
In an interview on 05/09/24 at 10:52 am, LVN B stated Resident #241 got IV antibiotics every 8 hours. The
medication ran for four hours, and after the four hours, the tubing was capped with the alcohol green cap. If
the PICC dressing had a bio patch under it, it was to be changed every 7 days. If there was no bio patch, it
was to be changed every 3 days. EBP means staff was to wear a gown with any contact with resident and
any time dressings were changed or wound care/device care was done.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Record review of the facility's Dressing Change for Vascular Access Devices policy/procedure dated
08/2021 stated in part:
-Central venous access device and midline dressing changes will be done at established intervals and
immediately if the integrity of the dressing is compromised, if moisture, drainage or blood is present, or for
further assessment if infection is suspected.
-Transparent semi-permeable membrane dressings are changed every 7 days and PRN.
-If a chlorhexidine impregnated gauze sponge (Bio patch) is applied under the transparent dressing,
change every 7 days.
-If a patient is allergic to the transparent dressing and a gauze and tape dressing is used over the site, the
gauze dressing must be changed every 48 hours and PRN. Gauze underneath a transparent
semi-permeable membrane dressing is considered a gauze dressing.
-A dressing is changed immediately if:
-The dressing is non-occlusive or soiled.
-If using a catheter securement device (Stat lock) it must be changed with each dressing change.
Record Review of the facility's Central Line Dressing Change check off (not dated) stated:
-Gather the necessary equipment:
Antiseptic (chlorhexidine preferred)
Sterile transparent semipermeable dressing (may be chlorhexidine impregnated)
Or sterile 4 x 4 gauze pad
Sterile tape
Sterile drape
Alcohol free skin barrier solution
Sterile gloves
Gloves
Masks x2 (1 for nurse and 1 for the client)
Label
Sterile needless connectors (saline/ heparin lock)
Sterile disinfectant caps
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Sterile, preservative free, prefilled syringes with 10 mL 0.9% normal saline
Level of Harm - Minimal harm
or potential for actual harm
(Number of syringes required based on number of lumens of the CVAD)
Residents Affected - Few
*Many facilities have sterile pre-packaged CVAD dressing kits that contain the necessary supplies for a
CVAD dressing change. Use of pre-packaged kits is recommended when available.
-Follow manufacturer's recommendations for cleansing, application, and dry times:
Follow manufacturer's recommendations for appropriate cleansing products, application, and dry times.
Always allow the product to dry naturally without wiping, fanning, or blowing on the skin. Cleansing products
are typically applied using back and forth motion while moving vertically and horizontally for at least 30
seconds.
-Open the needleless connector package:
Open the needleless connector package using sterile technique and inspect the integrity of the device.
Attach the prefilled 10mL normal saline syringe and prime the connector.
-Ensure the clamp between the connector and the catheter is closed
-Remove the existing needleless connector and scrub the catheter hub:
Remove the existing needleless connector. Perform a vigorous scrub of the catheter hub per facility policy.
Allow it to dry completely.
-Attach the new primed needleless connector:
Attach the new primed needleless connector to the catheter hub and rotate to tighten.
-Unclamp the catheter and aspirate for a blood return:
Unclamp the catheter and aspirate for a blood return. If blood is aspirated, slowly inject the normal saline
flush into the catheter using a pulsatile flushing technique.
-Clamp the catheter and remove the syringe
-Place a new antiseptic-impregnated sterile port cap:
Place a new antiseptic-impregnated sterile port cap on the needleless connector, if available.
Record review of the facility's Enhanced Barrier Precautions signage that was outside the entry doors of
residents that required Enhanced Barrier Precautions states in part:
-Providers and staff must also:
Wear gloves and a gown for the following High-Contact Resident Care Activities.
Device care or use:
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
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
455925
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Veranda Rehabilitation and Healthcare
4301 S Expressway 83
Harlingen, TX 78550
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 0880
Central line.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455925
If continuation sheet
Page 11 of 11