Central Admixture Pharmacy Services recalls fentanyl syringes with specific lot numbers due to lack of sterility assurance from sanitization cycles. Consumers should contact the manufacturer for details.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services has recalled specific fentanyl syringes because their sanitization cycles weren't validated for sterility. This could lead to infections if the syringes are used without proper sterility.
The syringes were made without validated sanitization cycles, meaning they might not be sterile. This could cause infections if used in medical procedures without proper sterility checks.
Healthcare professionals and patients using the recalled fentanyl syringes for medical purposes. Those with the specific lot numbers listed are most at risk.
Check the lot numbers on the syringe: 17-270813 through 17-273687, with expiration dates from July 19, 2023, to September 6, 2023. The product is a fentanyl injection syringe for prescription use.
Look for lot numbers 17-270813 to 17-273687 on the syringe label.
The product is not safe to use as it lacks validated sterility assurance, which could lead to infections.
The official recall notice does not specify a replacement process.
Contact Central Admixture Pharmacy Services, Inc. at 7935 Dunbrook Road, Suite C, San Diego, CA 92126 for further instructions.
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-1062-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1062-2023 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.