Central Admixture Pharmacy Services recalls vancomycin IV bags with potential sterility issues. These bags may not be sterile, risking infections during medical treatment.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled certain vancomycin IV bags because they lack proper sterility assurance. This could lead to infections if used in medical treatments.
The recall states that validation data for decontamination cycles is lacking, meaning the bags may not be sterile. This could cause infections during medical procedures if the bags are used without proper sterility.
Healthcare providers and patients receiving vancomycin injections through these specific IV bags. Those with the listed lot numbers and expiration dates are most at risk.
Check for the lot numbers 36-239524 through 36-255124 and expiration dates listed in the recall notice. These bags are labeled as vancomycin 1.5 g/250 mL added to 0.9% sodium chloride, 6 mg/mL, IV bags.
Identify the lot number and expiration date on the IV bag to determine if it is part of the recall.
The recall states that validation data for decontamination cycles is lacking, which means the bags may not be sterile.
The recall does not specify a remedy, so check the product details to see if it matches the listed lot numbers and expiration dates.
Yes, the recall includes lot numbers 36-239524 through 36-255124 with specific expiration dates listed in the notice.
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-0966-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0966-2023 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.
