Central Admixture Pharmacy Services recalls fentanyl 100mL bags due to lack of sterility assurance from sanitization cycles. Affected lots expire 8/2023 or 9/2023. Contact for details.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl 100mL bags that may not be sterile due to insufficient sanitization validation. This poses a risk of infection during medical use, so affected users should stop using the product immediately.
The bags lack validated sanitization cycles, meaning they might not be sterile when used in medical settings. This could lead to infections or other complications for patients receiving the medication.
Healthcare facilities and medical professionals using the recalled fentanyl bags for patient treatment. Those handling the specific lots listed in the recall are most at risk.
Check for the lot numbers 17-273074 (expiring 8/28/2023) or 17-273772 (expiring 9/7/2023) on the fentanyl bags. The product is a 100mL bag labeled for prescription use only.
Discard the recalled fentanyl bags with lot numbers 17-273074 or 17-273772 as they may not be sterile.
The recall record does not provide a specific recall number.
Check the lot number on the bag; affected lots are 17-273074 (expiring 8/28/2023) or 17-273772 (expiring 9/7/2023).
Yes, contact Central Admixture Pharmacy Services, Inc. at 7935 Dunbrook Road, Suite C, San Diego, CA 92126 for further assistance.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-1051-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1051-2023 from Central Admixture Pharmacy Services. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
