Fagron recalls fentanyl citrate IV bags due to lack of assurance of sterility. This could cause infections if used improperly. Affected units have specific lot numbers and expiration dates.
Lack of Assurance of Sterility
Fagron Compounding Services is recalling fentanyl citrate IV bags because they may not be sterile. Using these bags could lead to infections, especially in medical settings where sterile solutions are critical.
The bags may not be sterile, which can lead to infections if used in medical procedures. Fentanyl is a potent opioid used for pain management, so any contamination could cause serious health issues.
Healthcare providers and patients receiving IV fentanyl treatment are most at risk. The recall affects specific lot numbers of fentanyl citrate bags sold in the U.S.
Check for the lot number C274-000040409 and expiration date 03/22/2025 on the bag. The product is a single-use 100mL IV bag labeled as Fagron Sterile.
Look for the lot number C274-000040409 and expiration date 03/22/2025 on the IV bag.
The recall indicates a lack of assurance of sterility, so it is not safe to use. The product may cause infections if used.
The recall does not specify a remedy, so contact Fagron Compounding Services for guidance.
Check for the lot number C274-000040409 and expiration date 03/22/2025 on the IV bag.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0225-2025 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0225-2025 from Fagron. 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.
