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 that all drugs and medical
devices used in the facility were labeled in accordance with professional standards, including expiration
dates for 2 of 2 medication rooms, 2 of 3 medication carts, and 1 of 2 treatment carts observed for
expirations dates.
The facility had expired Central Line Dressing Kits in the west and east wing medication rooms, and expired
medications in the A-hall/B-hall medication carts and the east wing treatment cart.
These failures could place residents at risk for infection, a serious drug reaction or not receiving the
intended therapeutic benefit of medication.
The findings were:
Observation of the west wing medication room on 01/22/23 at 01:07 PM revealed the following items:
6 expired Central Line Dressing Kits:
2 expired on 06/30/22,
1 expired on 09/30/22, and
3 expired on 12/31/22.
Observation of the east wing medication room on 01/22/23 at 01:10 PM revealed the following items:
14 expired Central Line Dressing Kits:
5 expired on 08/31/22,
3 expired on 09/30/22, and
5 expired on 12/31/22.
An interview with the ADON on 01/22/23 at 01:12 PM, the ADON stated there were no residents with
central lines at this time; the last one was some time ago. The ADON stated she was in the process of
consolidating the supplies to a central location. The ADON stated she was responsible for checking
(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 3
Event ID:
455608
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
455608
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/24/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Hacienda Oaks at Beeville
4713 Business 181 N
Beeville, TX 78102
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
the med rooms and central supply and thought the central line dressing kits were only in the central supply,
but there were none in the central supply. The ADON stated that staff get and stash them for easier access.
The ADON stated it was important that central line dressing kits were not expired because using the
contents could cause infection.
Observation on 01/23/23 at 03:10 PM of the A Hall medication cart with the DON revealed an approximate
half bottle of 1000 stool softener tablets expired as of 12/22.
Observation on 01/23/23 at 03:12 PM of the B-Hall medication cart with the DON was an opened 100ml
(milliliter) bottle of normal saline that was undated, timed, or initialed.
Observation on 01/23/23 at 03:14 PM of the east wing treatment cart revealed a partial 8-ounce spray
bottle of wound cleanser that expired on 12/22.
An interview with the DON on 1/23/23 at 03:15 PM revealed it was important not to administer expired
medications because the expiration dates were there for a reason. The DON stated the medications could
lose their potency or cause an unexpected reaction because their chemical makeup could be altered after
the expiration dates.
According to the FDA website, drug expiration dates reflect the time period during which the product is
known to remain stable, which means it retains its strength, quality, and purity when it is stored according to
its labeled storage conditions. If a drug has degraded, it might not provide the patient with the intended
benefit because it has a lower strength than intended. In addition, when a drug degrades it may yield toxic
compounds that could cause consumers to experience unintended side effects.
Sterility may be compromised after the expiration date on medical devices such as IV tubing, catheters, and
other sterilized products.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455608
If continuation sheet
Page 2 of 3
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
455608
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/24/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Hacienda Oaks at Beeville
4713 Business 181 N
Beeville, TX 78102
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 0912
Level of Harm - Potential for
minimal harm
Residents Affected - Many
Provide rooms that are at least 80 square feet per resident in multiple rooms and 100 square feet for single
resident rooms.
Based on observation, interview, and record review, the facility failed to provide the required 80 square foot
per resident in 48 of 48 multiple resident rooms (1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18,
19, 20, 21, 22, 23, 24, 25, 27, 28, 29, 30, 31, 33, 34, 35, 36, 37, 38, 39, 41, 42, 43, 44, 45, 46, 48, 49, 50,
51, and 52.
All 48 facility multiple resident rooms did not have the required square footage.
This deficient practice could affect residents who resided in rooms with less than the required square
footage and make it difficult for the residents to move around in their rooms.
The findings were:
Review of Health and Human Services Form 3740 Bed Classifications, dated 01/22/2023, revealed 44
rooms with two beds and four rooms (23, 24, 51, and 52) with three beds.
Beginning at 1:30 p.m. on 10-29-19 during the facility's previous recertification survey, this surveyor, using
an agency laser measuring device, obtained measurements for all 48 resident rooms. Rooms with two beds
measured between 149.0 and 156.5 square feet. Rooms with three beds measured between 220.1 and
220.9 square feet. None of the bedrooms measured provided the required 80 square feet per resident.
On 01/22/2023, the Administrator provided a letter requesting a room size waiver.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455608
If continuation sheet
Page 3 of 3