Central Admixture Pharmacy Services recalls vancomycin IV bags due to lack of sterility assurance. These bags may contain contaminants that could cause infection if used in medical treatments.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling vancomycin IV bags that were added to dextrose 5% solution. The bags lack proper sterility validation, which could lead to infections if used in medical treatments.
The bags were produced without sufficient validation of their decontamination cycles, meaning they might not be sterile. This lack of sterility could introduce harmful bacteria into the bloodstream during medical procedures, potentially causing infections.
Healthcare professionals who use these vancomycin IV bags for patient treatment are most at risk. Patients receiving the medication through these bags could be exposed to contaminants.
Check for the NDC number 72196-6073-1 on the bag. The lot numbers listed (36-245562 to 36-251727) and expiration dates (from July 10, 2023, to August 29, 2023) indicate which batches were affected.
Look for the NDC number 72196-6073-1 and the listed lot numbers on the bag.
The recall is due to a lack of assurance of sterility in the bags, as validation data for decontamination cycles is missing.
The official recall notice does not specify a remedy, so contact the manufacturer for guidance.
Yes, the affected products have expiration dates ranging from July 10, 2023, to August 29, 2023.
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-0950-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0950-2023 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.
