Central Admixture Pharmacy Services recalls vancomycin IV bags due to lack of sterility assurance. These bags may cause infections if used in medical treatments. Contact for details.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services recalls specific vancomycin IV bags because they lack proper sterility validation. Using these bags could lead to infections in patients receiving intravenous treatment.
The bags were manufactured without sufficient validation of their decontamination cycles, meaning they might not be sterile. This lack of sterility could lead to infections in patients during intravenous treatments.
Healthcare facilities using these vancomycin IV bags for intravenous treatments are affected. Patients receiving the medication are at risk of infection if the bags are used without proper sterility.
Check for the NDC code 72196-6071-1 on the bag. The lot numbers range from 36-239990 to 36-255691 with expiration dates from July 2023 through September 2023.
Identify the NDC code 72196-6071-1 and lot numbers 36-239990 to 36-255691 on the bag.
Central Admixture Pharmacy Services recalls specific vancomycin IV bags due to lack of sterility validation.
Check for NDC code 72196-6071-1 and lot numbers 36-239990 to 36-255691 with expiration dates from July 2023 through September 2023.
The recall record does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
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-0971-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0971-2023 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.
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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.
