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Inspection visit

Health inspection

FOCUSED CARE AT ORANGECMS #6760941 citation on this visit
1 citation recorded

Inspector’s narrative

What the inspector wrote

This survey cited 1 deficiency. The full statement and the facility’s plan of correction follow, verbatim from the federal record.

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

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Citations

1 citation recorded*CMS

What do CMS severity letters mean?

Serious (G-L). Actual harm to a resident, or immediate jeopardy. Codes G through I indicate actual harm; J through L indicate immediate jeopardy to resident health or safety.

General (A-F). No actual harm found, or harm that is minimal. The facility must still submit a Plan of Correction. Most CMS citations land here.

Each letter combines severity with scope: how many residents the deficiency affected.

  • 0760GeneralS&S Epotential for harm

    F760 - Residents are free of any significant medication errors

    Ensure that residents are free from significant medication errors.

FAQ · About this visit

Common questions about this visit

What happened during the November 18, 2025 survey of FOCUSED CARE AT ORANGE?

This was a inspection survey of FOCUSED CARE AT ORANGE on November 18, 2025. The surveyor cited 1 deficiency, recorded on the federal Form 2567 statement of deficiencies.

Were any deficiencies cited at FOCUSED CARE AT ORANGE on November 18, 2025?

Yes, 1 deficiency was cited, each with a CMS Scope and Severity grade. The first was: "Ensure that residents are free from significant medication errors."

What type of survey was this?

This was a inspection survey conducted by state surveyors under federal Centers for Medicare & Medicaid Services (CMS) oversight. Findings are published on CMS Care Compare.

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Next steps

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Data from CMS Care Compare public records. Dataset last refreshed . If you believe any information is inaccurate, report it here.