Central Admixture Pharmacy Services recalls NORepinephrine added to 0.9% sodium chloride solutions because FDA found potential sterility issues in products intended to be sterile.
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 added to 0.9% sodium chloride. The recall is due to an FDA inspection finding possible sterility problems in products meant to be sterile, which could lead to infections if used improperly.
The products were intended to be sterile but an FDA inspection raised concerns about their sterility. If the solution is not sterile, it could cause infections when used in medical procedures.
Healthcare professionals using these solutions for medical purposes, particularly those in hospitals or clinics. Patients receiving these treatments are at risk if the solution is not sterile.
Check for the NDC number 71285-8096-1 on the packaging. The lot numbers listed include 37-882989 through 37-900362 with expiration dates from April 2023 to July 2023.
Look for the NDC number 71285-8096-1 and lot numbers listed in the recall notice.
An FDA inspection raised concerns about the sterility of these products, which are intended to be sterile but may not be safe for medical use.
Check the product details and lot numbers to see if it is affected. If it is, contact your healthcare provider for guidance.
The recall is due to potential sterility issues, which could lead to infections if used improperly, but the remedy is not specified in the 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-0744-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0744-2023 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.
