Recalled heparin IV bags from Central Admixture Pharmacy Services may lack sterility due to insufficient validation data for decontamination cycles. Affected lots expire through August 2023.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services recalled certain heparin IV bags that may not be sterile because their decontamination cycles weren't properly validated. This could lead to infections if used in medical treatments.
The heparin bags lack assurance of sterility because the validation data for cleaning cycles is missing. This means the bags could contain harmful bacteria or other contaminants that might cause infections when injected into patients.
Patients receiving IV heparin treatments at healthcare facilities using these specific lots are affected. Healthcare workers handling the product are at risk if they use contaminated bags.
Check the product label for the lot numbers listed: 36-243555 through 36-255488. These bags were sold with expiration dates from July 2023 through August 2023.
Look for lot numbers 36-243555 to 36-255488 on the heparin IV bag.
The heparin bags lack assurance of sterility because validation data for decontamination cycles is missing.
Check the product label for the lot numbers listed. If you have the affected lots, contact your healthcare provider for guidance.
The recalled heparin IV bags have lot numbers from 36-243555 to 36-255488 and expire between July 2023 and August 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-0978-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0978-2023 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.
