Central Admixture Pharmacy Services recalls NORepinephrine added to 0.9% sodium chloride for potential sterility issues. Products may not be sterile after FDA inspection.
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 NORepinephrine solutions that were compounded for medical use. The products were found to lack sterility assurance during an FDA inspection, which could lead to infections if used.
The FDA inspection found the products did not meet sterility standards. This means the solutions could be contaminated with bacteria, potentially causing infections if used in medical procedures.
Healthcare professionals and patients using the recalled NORepinephrine solutions for medical purposes. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name 'NORepinephrine added to 0.9% sodium chloride' with the specific lot numbers and expiration dates listed in the recall notice. The products are for prescription use only.
Look for the lot numbers and expiration dates listed in the recall notice to confirm if your product is affected.
The FDA inspection raised concerns about sterility, so the product is not safe for medical use. Do not use the recalled products.
Check the lot numbers and expiration dates to see if your product is affected. If it is, stop using it and contact the manufacturer for further instructions.
The recall notice does not specify a replacement process. Contact Central Admixture Pharmacy Services directly for assistance.
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-0745-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0745-2023 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.
