Central Admixture Pharmacy Services recalls fentanyl 100mL bags (NDC 71286-2003-5) with lot 17-275322 due to lack of sterility assurance. No remedy specified in recall notice.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl 100mL bags that may not be sterile. This could lead to infections if used improperly. The recall is for prescription-only products.
The recall states there is a lack of assurance of sterility. This means the fentanyl bags might not be sterile, which could cause infections if used in medical procedures. The hazard is specific to the manufacturing process.
Prescription patients using fentanyl 100mL bags from Central Admixture Pharmacy Services in San Diego. Healthcare providers preparing these medications are most at risk.
Check for the product name 'fentaNYL', 5,000 mcg/100 mL (50 mcg/mL), 100 mL Bag, Rx only. Look for the lot number 17-275322 and expiration date 10/3/2023 on the packaging.
Look for the lot number 17-275322 and expiration date 10/3/2023 on the fentanyl bag packaging.
The recall states there is a lack of assurance of sterility, so it may not be safe to use. No remedy is specified in the notice.
The recall notice does not specify any remedy or replacement options.
The expiration date is 10/3/2023 as listed in the product description.
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-0023-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0023-2024 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.
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.