F 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure it's free of any significant medication errors for 1 of
8 residents (Resident #1) reviewed for significant medication errors. The facility failed to identify Resident
#1 medication allergy to Hydrocodone and Resident #1 was administered 10 doses of Hydrocodone. This
failure could place residents at risk for having allergic reactions such as skin rashes, itching, or swelling if
given medications they are allergic to. Findings included: Record Review of Resident #1's face sheet dated
10/6/2025 indicated Resident #1 was a 78- year- old female initially admitted to the facility on [DATE] and
readmitted on [DATE] with diagnoses of Pain, Hyperlipidemia (high levels of fat in the blood.), and Primary
Hypertension (high blood pressure). Record review of Resident #1's Care plan dated 04/22/2025 indicated
Resident #1 had Codeine, Diazepam, Sulfa Antibiotics, Tramadol, Caffeine, Adhesive listed as her allergies
with Review listed allergies prior to administering new medications, and Give MD a list of allergies when
receiving orders to new medications listed as interventions. Record review of Resident #1's nurse's notes
and progress notes from the dates 04/23/2025- 05/05/2025 indicated there were no notes related to the
administration of Hydrocodone and any negative outcomes. Record review of Resident #1's Physician
orders dated 04/17/2025 indicated Hydrocodone was ordered by the hospital physician. Record Review of
Resident #1's Medication Record dated April 2025 indicated Resident # 1 had Codeine, Diazepam, Sulfa
Antibiotics, Tramadol, Caffeine, Adhesive listed for her allergies. Resident #1 received 10 doses of PRN (as
needed for pain) Hydrocodone -Acetaminophen Oral Tablet 5-325 MG related to pain. Dates & Times of
administration:- April 24, 2025 at 11:50 a.m. (administered by: LVN E)- April 25, 2025 at 3:45 p.m.
(administered by: LVN F)- April 25, 2025 at 10:43 p.m. (administered by: LVN F)- April 27, 2025 at 2:51 a.m.
(administered by: LVN G)- April 28, 2025 at 12:32 a.m. (administered by: LVN G)- April 28, 2025 at 12:24
p.m. (administered by: LVN E)- April 28, 2025 at 8:44 p.m. (administered by: LVN F)- April 29, 2025 at 11:50
a.m. (administered by: LVN E)- April 30, 2025 at 10:57 a.m. (administered by: LVN E)- April 30, 2025 at 8:00
p.m. (administered by: LVN F) Record review of nurse report sheet dated: 04/22/2025 retrieved by LVN A
indicated Resident #1 was allergic to Hydrocodone, Valium, Codeine, Clindamycin, Sulfa, and Tramadol and
adhesive tape. Record review of Resident #1's Hospital discharge paperwork dated 04/17/2025-04/22/2025
(length of hospital stay) indicated Hydrocodone was listed as an allergy. Record review of default progress
note entered by Nurse Practitioner B dated: April 30,2025 indicated Resident #1 had Hydrocodone listed as
one of her allergies. Record review of Residents with No Recommendations dated: 05/1/2025 thru
05/13/2025 indicated Resident #1 was reviewed by the pharmacy consultant with no recommendation
made. An interview on 10/07/2025 at 11:23 a.m. with Resident #1's family member indicated Family
Member A said she was not present during any time when Resident #1 received Hydrocodone. She said
she did not know how many doses were administered. Family Member A said she was told Resident #1
was allergic to Hydrocodone by Family Member B. She said Resident #1 wanted her to make the complaint
to
Residents Affected - Some
(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:
676094
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
676094
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/18/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Orange
4201 Fm 105
Orange, TX 77630
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 0760
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
State. Family Member A said she wanted all investigation findings and communications to be given to
Resident #1 and Family Member B. An interview on 10/07/2025 at 11:50 a.m. with Resident #1's family
member indicated Family Member B said when Resident #1 was admitted on [DATE] she reported to the
staff that Resident #1 was allergic to Hydrocodone. Family Member B said she was aware that Resident #1
had a urinary tract infection during her stay at the facility. Family Member B could not recall the name of the
staff member she reported Resident #1 allergies too. She said Resident #1 reported to her that she was not
forced to take the Hydrocodone but was told the Hydrocodone would not affect her because she would be
sleeping. Family Member B said she was not present at any of the times Hydrocodone was administered.
An interview on 10/07/2025 at 12:07 p.m. indicated Nurse Practitioner C said a person with a true
medication allergy could have a skin rash, itching, hives, and or shortness of breath. She said people
sometimes list medications they did not like taking under allergies, so they would not be given the
medication even though it was not a true allergy. She said she would not have approved a resident with an
allergy to Hydrocodone to receive Codeine to prevent a potential allergic reaction. Nurse Practitioner C said
Resident #1 was given Hydrocodone first during her 04/17/2025 hospital stay before admitting to facility.
and was not ordered Hydrocodone by the facility. Nurse Practitioner C said she cannot prescribe
Hydrocodone, only the Physician can. She cannot recall if Resident #1 had any skin rashes, itching, hives,
or shortness of breath, or negative effects from receiving 10 doses of Hydrocodone. An interview on
10/07/2025 at 2:00 p.m. indicated Pharmacist #1 said a true medication allergy is different from a side
effect. He said most common symptoms of drug allergy are hives, rash, itching and fever. Pharmacist #1
said if a resident has a true drug allergy, they could potentially experience hives, rash, and itching. He said
he would not recommend residents with a Codeine or Hydrocodone allergy to receive a dose of
Hydrocodone. An interview on 10/07/2025 at 2:45 p.m. indicated the ADON said Resident #1's Medication
administration record showed she was given 10 doses of Hydrocodone Oral Tablet 5-325 MG. The ADON
said she reviewed Resident #1's allergies and said she should not have been given Hydrocodone. She said
the potential harm to Resident #1 receiving Hydrocodone could be her having skin hives, skin rashes, and
or itching. An interview on 10/07/2025 at 2:55 p.m. indicated the Administrator said Resident #1 had an
allergy to Hydrocodone and should not have been given any Hydrocodone. She said Resident #1 could
have had an allergic reaction causing her itching, skin rashes, and or skin hives. An interview on
10/08/2025 at 1:00 p.m. indicated Resident #1 said she did not know she had received a dose of
Hydrocodone in the hospital. She said she didn't know she had received 10 doses of Hydrocodone at the
facility. Resident #1 said staff did inform and educate her on medications before administering them to her.
Resident #1 said she had a lot of allergies and had an active urinary tract infection during her 04/23/2025
stay at the facility. Resident #1 said she was not forced to take Hydrocodone. Resident #1 said she didn't
know she had mental disturbances when she took the Hydrocodone. She said Family Member B told her
she had mental disturbances when she took Hydrocodone. Resident #1 said when she was admitted to the
facility, Family Member B told staff she was allergic to Hydrocodone. Resident #1 could not recall which
staff her family member reported her allergies to. Record review of In- service training report on the topic of
Allergies dated: 05/13/2025 indicated When getting new medication orders make sure to check the
residents' allergies. If resident is allergic ask for alternative medication. Conducted by the Director of
Nurses. Record review of the facility's policy General Guidelines for Medication Administration. revision
dated: 08/2020 indicated (in part):Policy: Medications are administered as prescribed in accordance with
good nursing principles and practices and only by persons legally authorized to administer.7. a.- Working
with the resident or their representative and appropriate
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676094
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
676094
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/18/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Orange
4201 Fm 105
Orange, TX 77630
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 0760
Level of Harm - Minimal harm
or potential for actual harm
clinicians (i.e., the consultant pharmacists, attending physician, medical director, etc.) the facility should
determine the most appropriate method for administering medications that considers each resident's safety,
needs, medications, schedule, preferences, and functional ability.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676094
If continuation sheet
Page 3 of 3