Central Admixture Pharmacy Services recalls heparin solutions that may not be sterile, posing a risk of infection. Affected products include specific lot numbers and expiration dates.
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 has recalled heparin solutions that were found to lack sterility during an FDA inspection. Using these products could lead to infections in patients receiving them.
The FDA inspection found the heparin solutions were not sterile, meaning they could introduce harmful bacteria into the bloodstream. This poses a serious infection risk for patients undergoing medical treatments.
Healthcare professionals and patients receiving heparin treatments through central lines. Those using the recalled products for medical purposes are at risk of infection.
Check for lot numbers 37-888833 through 37-895758 with expiration dates between May 2023 and May 2023. These products were sold as heparin added to 0.9% sodium chloride for medical use.
Immediately discard any heparin solutions with the listed lot numbers and expiration dates.
The FDA inspection found the heparin solutions were not sterile, which could lead to infections in patients.
Lot numbers 37-888833, 37-890537, 37-892161, 37-892163, 37-893979, 37-893992, 37-895755, and 37-895758.
Check the lot number and expiration date on the product label. Affected products have specific lot numbers and expiration dates listed in the recall notice.
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-0746-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0746-2023 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.
