Central Admixture Pharmacy Services recalls heparin solutions due to potential contamination. Products may not be sterile, posing risks during medical use. Check NDC numbers and expiration dates for affected lots.
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 potentially contaminated. This could lead to infections if used in medical treatments, especially in sterile procedures.
The FDA found that the heparin solutions might not be sterile, which could cause infections during medical procedures. This is a serious issue because heparin is used in critical treatments like blood thinning.
Healthcare professionals and patients receiving heparin treatments through these specific solutions. Those using the recalled products for medical purposes are most at risk.
Check for NDC numbers 71285-7009-1 and expiration dates listed in the recall notice. The affected lots include specific numbers with expiration dates from May 2023.
Verify the NDC number and expiration date on the product label to see if it matches the recalled lots.
The FDA found that the heparin solutions might not be sterile, which could lead to infections during medical procedures.
The recall does not specify a remedy, so check the product details to see if it matches the recalled lots and contact your healthcare provider for guidance.
Yes, the recalled products have expiration dates from May 2023, including specific lot numbers with dates like 05/02/2023 and 05/30/2023.
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-0726-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0726-2023 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.
