CAPS recalls specific peripheral parenteral nutrition bags due to insufficient cleaning documentation in the compounding area, potentially affecting safety. This recall involves refrigerated injection products with specific lot numbers.
Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
Central Admixture Pharmacy Services (CAPS) recalls certain peripheral parenteral nutrition bags because the compounding process lacked proper cleaning documentation. This could lead to inconsistent product safety if the bags are used without proper sterility.
The compounding area was identified as an ISO-5 environment where daily cleaning steps were not properly documented. This lack of documentation could result in inconsistent sterility during the preparation of the medication, potentially affecting patient safety.
Patients receiving prescription peripheral parenteral nutrition from CAPS in Los Angeles are affected. Healthcare providers using these specific bags for medical treatments are most at risk.
Check for the specific lot numbers: 11-4785290-0-1 (1440 mL bag) or 11-4785217-0-1 (1700 mL bag). These products were sold by CAPS in Los Angeles with a 2025 expiration date.
Look for lot numbers 11-4785290-0-1 or 11-4785217-0-1 on the bags.
The recalled products are peripheral parenteral nutrition bags (1440 mL and 1700 mL) with specific lot numbers: 11-4785290-0-1 and 11-4785217-0-1.
The recall was issued because the compounding area did not have sufficient documentation for a daily cleaning step, which could affect product sterility.
Check the lot numbers on the bag: 11-4785290-0-1 (1440 mL) or 11-4785217-0-1 (1700 mL). These products were sold by CAPS in Los Angeles with a 2025 expiration date.
We’ve drafted a message you can send CAPS to request your refund or repair — edit it as you like.
Subject: Recall D-0530-2025 — CAPS CAPS Hello, I own a CAPS that is covered by recall D-0530-2025 from CAPS. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
