Central Admixture Pharmacy Services recalls heparin IV bags due to lack of sterility validation. Affected units have NDC 72196-8100-1 and lots 36-260045/36-260046. Contact for return instructions.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services recalls heparin IV bags that may not be sterile. This could lead to infections if used in medical treatments. Patients and healthcare providers should stop using these bags immediately.
The heparin bags lack validated sanitization cycles, meaning they might not be sterile. If used in medical procedures, this could cause infections or other health issues.
Healthcare providers and patients using the recalled heparin IV bags for medical treatments. Those with the specific NDC number and lot numbers are most at risk.
Check for NDC number 72196-8100-1 and lot numbers 36-260045 or 36-260046 on the IV bag. These bags were sold with expiration date 9/13/2023.
Discontinue use of the recalled heparin IV bags as they may not be sterile and could cause infections.
The NDC number is 72196-8100-1.
Lot numbers 36-260045 and 36-260046 are affected.
The heparin bags expired on 9/13/2023.
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-1135-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1135-2023 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.
