Central Admixture Pharmacy Services recalls fentanyl 250mL bags with specific lot numbers due to lack of sterility assurance. This could lead to infections if used improperly.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl 250mL bags that were prepared for medical use. The recall is because these bags might not be sterile, which could cause infections if used in medical procedures.
The fentanyl bags may not be sterile, meaning they could introduce harmful bacteria into the bloodstream during medical procedures. This poses a risk of infection, but the risk is not immediate or severe under normal use conditions.
Healthcare professionals using these fentanyl bags for medical procedures are affected. Patients receiving the medication through these bags are at risk of infection if the bags are not sterile.
Check for the lot numbers 17-275517, 17-275862, 17-275980, or 17-276036 on the bag. These bags were manufactured by Central Admixture Pharmacy Services, Inc. and expire by October 5, 2023, through October 16, 2023.
Look for lot numbers 17-275517, 17-275862, 17-275980, or 17-276036 on the fentanyl bag.
The fentanyl bags may not be sterile, which could lead to infections if used in medical procedures.
The official recall notice does not specify a remedy, so contact Central Admixture Pharmacy Services, Inc. for guidance.
Check for lot numbers 17-275517, 17-275862, 17-275980, or 17-276036 on the bag.
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-0014-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0014-2024 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.
