Central Admixture Pharmacy Services recalls vancomycin IV bags with potential sterility issues. Lack of validation data for decontamination cycles poses a risk of contamination.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled certain vancomycin IV bags due to a lack of validation data for decontamination cycles. This could lead to contamination risks if the bags are used in medical settings.
The recalled vancomycin bags lack sufficient validation data for decontamination cycles, which could result in contamination. This poses a risk of infection or other complications if the bags are used in medical settings without proper sterility.
Healthcare professionals and patients receiving vancomycin treatment through intravenous infusion are affected. Those using the recalled bags for medical purposes are at risk of contamination.
Check for the NDC number 72196-6064-1 and lot numbers 36-245576 through 36-256045 on the packaging. The bags were sold with expiration dates from July 2023 to September 2023.
Identify the NDC number 72196-6064-1 and lot numbers listed in the recall notice to confirm if your bag is affected.
The recall is due to a lack of validation data for decontamination cycles, which could lead to contamination risks.
The official recall notice does not specify a remedy, so contact Central Admixture Pharmacy Services for further instructions.
Yes, the recalled bags have expiration dates ranging from July 12, 2023, to September 11, 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-0948-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0948-2023 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.
