Central Admixture Pharmacy Services recalls fentanyl 100mL bags due to lack of sterility assurance. This could lead to infections if used improperly. Affected units have specific NDC and lot numbers.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl 100mL bags because they may not be sterile. Using these bags could lead to infections if they are not properly handled.
The bags may not be sterile, which means they could introduce harmful bacteria into the bloodstream during medical procedures. This poses a risk of infection, especially in critical care settings.
Healthcare facilities using these fentanyl bags for medical treatments are most at risk. Patients receiving injections from these bags could be exposed to infection.
Check for the NDC number 71286-2003-4 and lot number 17-275704 on the bag. The expiration date is October 9, 2023.
Look for the NDC number 71286-2003-4 and lot number 17-275704 on the fentanyl bag.
The recall indicates a lack of sterility assurance, so these bags should not be used until the remedy is applied.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
Check for the NDC number 71286-2003-4 and lot number 17-275704 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-0022-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0022-2024 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.
