Central Admixture Pharmacy Services recalls EPINEPHrine added to 0.9% sodium chloride for potential contamination. Products may not be sterile, risking infection after administration. Discard affected lots immediately.
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 EPINEPHrine solutions mixed with 0.9% sodium chloride due to concerns about sterility after an FDA inspection. Using these products could lead to infections since they are intended to be sterile.
The products were found to lack sterility during an FDA inspection. This means the solutions could contain harmful bacteria or other contaminants that might cause infections when injected or administered into the body.
Healthcare professionals and patients using the recalled EPINEPHrine solutions for medical purposes. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the lot numbers listed: 37-882988 through 37-899304. These are specific batches of EPINEPHrine added to 0.9% sodium chloride for medical use.
Remove all recalled EPINEPHrine solutions from storage and dispose of them safely to prevent potential infection.
The FDA found that the products lacked sterility after an inspection, meaning they could contain harmful contaminants that cause infections when used.
Discard the product immediately and contact your healthcare provider for guidance on alternative treatments.
Yes, check the product label for lot numbers between 37-882988 and 37-899304, which are 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-0742-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0742-2023 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.
