Central Admixture Pharmacy Services recalls fentanyl injection vials with potential lack of sterility. Affected lots expire by October 2023. Consumers should contact the manufacturer for details.
Lack of assurance of sterility:
Central Admixture Pharmacy Services has recalled fentanyl injection vials that may not be sterile. This could lead to infections if used improperly. The recall affects specific lots produced between 2023 and 2024.
The vials may not be sterile, which could cause infections if used in medical procedures. This is a serious concern for patients receiving injections but is not a direct risk to the general public.
Healthcare professionals using the recalled fentanyl vials for medical treatments are most at risk. Patients receiving these injections through healthcare facilities may also be affected.
Check for the lot numbers listed: 17-275314 through 17-276103. The vials expire by October 2023. They are labeled as fentanyl in 0.9% sodium chloride solution for medical use only.
Reach out to Central Admixture Pharmacy Services, Inc. at 7935 Dunbrook Road, Suite C, San Diego, CA 92126 for specific instructions.
The recall indicates a potential lack of sterility, so it is not safe to use. The manufacturer recommends contacting them for details.
Contact Central Admixture Pharmacy Services, Inc. directly for instructions on how to handle the product.
Check the lot numbers listed in the recall: 17-275314 through 17-276103. The vials expire by October 2023.
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-0012-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0012-2024 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.
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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.
