Central Admixture Pharmacy Services recalls heparin solutions for potential contamination. Products may not be sterile, posing risks during medical use. Check lot numbers and contact for details.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling heparin solutions that were found to lack sterility assurance during an FDA inspection. This could lead to infections if used in medical procedures.
The FDA inspection raised concerns about the sterility of these heparin solutions, which are intended for sterile medical use. If contaminated, they could cause infections in patients during medical procedures.
Healthcare professionals using these heparin solutions in hospitals or clinics are most at risk. Patients receiving the product could face infections if the solution is not sterile.
Check for lot numbers 37-888736, 37-888769, 37-890465, 37-890483, 37-892088, 37-892117, 37-892119, 37-892145, 37-893759, 37-893765, 37-895742, 37-895751, and expiration dates up to May 2023.
Identify the lot numbers on the heparin solution packaging to determine if it is part of the recalled batch.
The FDA inspection raised concerns about the sterility of these heparin solutions, which are intended for sterile medical use.
If not sterile, the product could cause infections in patients during medical procedures.
Check the lot numbers listed in the recall notice: 37-888736, 37-888769, 37-890465, 37-890483, 37-892088, 37-892117, 37-892119, 37-892145, 37-893759, 37-893765, 37-895742, 37-895751.
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-0732-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0732-2023 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.
