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Inspection visit

Health inspection

Valley Vista Post AcuteCMS #0555002 citations on this visit
2 citations recorded

Inspector’s narrative

What the inspector wrote

This survey cited 2 deficiencies. The full statement and the facility’s plan of correction follow, verbatim from the federal record.

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 expired oral medications and topical creams were removed from the current medication supplies. In addition, nasal sprays, eye drops, and pain patches were commingled with the current medication supplies readily available for residents' use. Also, the medication room temperature was not consistently monitored as required. These failures had the potential for unsafe storage of medications thereby losing the efficacy of the medications. Findings: 1a. On 9/4/19 at 9:32 A.M., a medication storage inspection of the treatment cart and interview was conducted with Licensed Nurse (LN) 1. The treatment cart had five drawers. In the first drawer, there was half a box of individual packets of hydrocortisone cream (topical medication used to help relieve redness, itching, swelling) with an expiration date of 8/19. In the fifth drawer, there was one opened tube of benzoyl peroxide 10 % (medication used to treat mild to moderate acne) with an expiration date of 9/18, and one tube ointment of a soothe and cool barrier (moisture ointment) with an expiration date of 8/19. LN 1 stated the LNs should have been checking at the expiration date of the medications and discarded the expired treatment medications. LN 1 acknowledged the policy and guidelines on storage of medications should have been followed. On 9/5/19 at 2:10 P.M., an interview was conducted with the Director of Nursing (DON). The DON LNs should have checked the treatment and medication carts to ensure medications were current. A review of the facility's policy titled, Storage and Expiration of Medications, Biologicals, Syringes and Needles, revised 10/31/16, indicated, Procedure . 3. General Storage Procedures: . 3.2 Facility should ensure that external use medications and biologicals are stored separately from internal use medications and biologicals . 5. Once any medication or biological package is opened, Facility should follow the manufacturer/ supplier guidelines with respect to expiration dates for opened medications . 5.2 Medications with a manufacturer's expiration date expressed in month and year (e.g. May 2019) will expire on the last day of the month . 2. On 9/4/19 at 10:17 A.M., a medication storage inspection, interview, and record review was conducted with LN 1. There were 15 missing signatures in the medication room temperature log in PM shifts. The dates were identified as follows: 1/3, 1/5, 1/7, 1/8, 1/9, 1/15, 1/16, 1/17, 1/21, 1/27, 1/29, (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 4 Event ID: 055500 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 055500 B. Wing A. Building (X3) DATE SURVEY COMPLETED 09/06/2019 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Valley Vista Post Acute 1025 W. Second Avenue Escondido, CA 92025 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 4/11, 4/12, 4/14, and 4/15/19. Level of Harm - Minimal harm or potential for actual harm LN 1 stated the medication room temperature should have been checked and monitored by the LNs twice a day for a potential that temperature would be out of range. LN 1 also stated LNs should have monitored the temperature consistently to maintain the effectiveness and potency of the medications. Residents Affected - Some On 9/5/19 at 2:10 P.M., an interview was conducted with the Director of Nursing (DON). The DON further stated the medication room temperatures should have been monitored twice a day consistently to ensure the potency of the medications. The DON stated who knows the temperature was off and could affect the medications' effectiveness. A review of the facility's policy titled, Storage and Expiration of Medications, Biologicals, Syringes and Needles, revised 10/31/16, indicated, Procedure . 3. General Storage Procedures: .11. Facility should ensure that medications and biologicals are stored at their appropriate temperatures according to the United States Pharmacopoeia guidelines for temperature ranges. 3a. On 9/4/19 at 12:03 P.M., a medication storage inspection of North medication cart and interview was conducted with LN 2. A half bottle of opened oral vitamin tablets was inside the drawer with an expiration date of 8/19. LN 2 stated the expired medications should have been removed from the cart. On 9/5/19 at 2:10 P.M., an interview was conducted with the Director of Nursing (DON). The DON stated the treatment cart and the medication cart should have been checked to ensure medications were organized and current. The DON stated it was missed and could potentially hurt the residents. A review of the facility's policy titled, Storage and Expiration of Medications, Biologicals, Syringes and Needles, revised 10/31/16, indicated, Procedure . 3. General Storage Procedures: .5. Once any medication or biological package is opened, Facility should follow the manufacturer/ supplier guidelines with respect to expiration dates for opened medications .5.2 Medications with a manufacturer's expiration date expressed in month and year (e.g. May 2019) will expire on the last day of the month . 3b. On 9/4/19 at 12:03 P.M., a medication storage inspection of the medication cart and interview was conducted with Licensed Nurse (LN) 1. Multiple medication supplies were commingled inside the drawer such as: Nasal sprays, eye drops, pain patches, and anticoagulant liquid medications. LN 2 stated she was not sure of the facility's policy related to the storage of nasal sprays, eyes drops, pain patches, and oral medications. LN 2 stated oral medications should have been separated from nasal sprays, eye drops, and patches for safety reasons. On 9/5/19 at 2:10 P.M., an interview was conducted with the Director of Nursing (DON). The DON stated LNs should have checked the treatment and medication carts to ensure the medications were organized and current. The DON stated it was missed and could potentially hurt the residents and storage of internal and external medications should have been separated. The DON also stated oral medications should have been separated from the other medications to prevent medication error and for infection control purposes. A review of the facility's policy titled, Storage and Expiration of Medications, Biologicals, Syringes and Needles, revised 10/31/16, indicated, Procedure . 3. General Storage Procedures: . 3.2 Facility should ensure that external use medications and biologicals are stored separately from internal (continued on next page) FORM CMS-2567 (02/99) Previous Versions Obsolete Event ID: Facility ID: 055500 If continuation sheet Page 2 of 4 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 055500 B. Wing A. Building (X3) DATE SURVEY COMPLETED 09/06/2019 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Valley Vista Post Acute 1025 W. Second Avenue Escondido, CA 92025 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 use medications and biologicals .5.2 Medications with a manufacturer's expiration date expressed in month and year (e.g. May 2019) will expire on the last day of the month . 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: 055500 If continuation sheet Page 3 of 4 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 055500 B. Wing A. Building (X3) DATE SURVEY COMPLETED 09/06/2019 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Valley Vista Post Acute 1025 W. Second Avenue Escondido, CA 92025 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 - Some 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 review of the Analysis of Client Accommodations, the facility failed to meet the required minimum square footage requirements of at least 80 square feet per resident (sq ft/resident) in 3 resident bedrooms (6, 8, and 11). This failure had the potential to impact resident care and quality of life. Findings: An observation from 9/3/19 through 9/5/19 was conducted during the survey. The following resident rooms contained less than 80 square feet for each resident: Room number Room Size 6 accommodated 3 residents 216 (72 sq ft/resident) 8 accommodated 3 residents 216 (72 sq ft/resident) 11 accommodated 2 residents 138 (69 sq ft/resident) Additionally, interviews and records reviews were conducted. There were no observed quality of care, or quality of life concerns that negatively affected the residents residing in the identified rooms during the recertification survey visit. A continuance of the waiver (variation) from the requirements of Code 42 of the Federal Regulations (CFR) section 483.70(d)(1)(ii) as granted, allowing less than 80 square feet per resident room, is hereby recommended. This recommendation is also made with the expectation that the facility will obtain a timely renewal of the current waiver granted by CMS. FORM CMS-2567 (02/99) Previous Versions Obsolete Event ID: Facility ID: 055500 If continuation sheet Page 4 of 4

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Citations

2 citations 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.

  • 0761GeneralS&S Epotential for harm

    F761 - Labeling of Drugs and Biologicals

    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.

  • 0912GeneralS&S Bno actual harm

    F912 - Measure at least 80 square feet per resident in multiple resident

    Provide rooms that are at least 80 square feet per resident in multiple rooms and 100 square feet for single resident rooms.

FAQ · About this visit

Common questions about this visit

What happened during the September 6, 2019 survey of Valley Vista Post Acute?

This was a inspection survey of Valley Vista Post Acute on September 6, 2019. The surveyor cited 2 deficiencies, recorded on the federal Form 2567 statement of deficiencies.

Were any deficiencies cited at Valley Vista Post Acute on September 6, 2019?

Yes, 2 deficiencies were cited, each with a CMS Scope and Severity grade. The first was: "Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted professional princip..."

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