Central Admixture Pharmacy Services recalls heparin IV bags with potential sterility issues. Products may not be sterile, risking infections during medical use. Affected lots and expiration dates listed.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling heparin IV bags that may not be sterile, which could lead to infections if used in medical treatments. This recall affects specific lots with expiration dates up to August 2023.
The heparin bags lack proper sterility validation, meaning they might contain contaminants that could cause infections when administered intravenously. This is a manufacturing issue with the decontamination process.
Healthcare professionals and patients receiving heparin treatments through IV infusion. Those using the recalled lots are most at risk.
Check for the NDC number 72196-8100-1 and lot numbers 36-243815 to 36-255957 on the packaging. The expiration dates range from July 11, 2023, to August 21, 2023.
Look for the NDC number 72196-8100-1 and lot numbers 36-243815 to 36-255957 on the heparin IV bag packaging.
The heparin bags lack validation data for decontamination cycles, which means they may not be sterile and could cause infections if used in medical treatments.
The recall record does not specify a remedy, so contact the manufacturer directly for guidance.
Yes, the products expire between July 11, 2023, and August 21, 2023, depending on the lot number.
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-0977-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0977-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
