Central Admixture Pharmacy Services recalls epinephrine IV bags with potential sterility issues. The product may not be sterile, risking infections during medical use. Affected units have specific lot numbers and expiration dates.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling epinephrine IV bags that may not be sterile, which could lead to infections if used in medical treatments. This recall affects healthcare professionals and patients receiving IV treatments.
The recall is due to insufficient validation data for sanitization cycles, meaning the bags may not be sterile. If used in medical settings, this could introduce infections into the patient's bloodstream, leading to serious health complications.
Healthcare professionals and patients receiving IV treatments using the recalled epinephrine bags. Those most at risk are individuals with compromised immune systems or those undergoing critical medical procedures.
Check for the lot number 36-260049 and expiration date 10/3/2023 on the IV bag. The product is labeled as epinephrine 2 mg added to dextrose 5% 250mL, concentration 8 mcg/mL, and is for prescription use only.
Look for the lot number 36-260049 and expiration date 10/3/2023 on the IV bag.
The recall indicates a lack of sterility assurance, so it is not safe to use. The product may cause infections if used in medical treatments.
The recall does not specify a remedy, so contact the manufacturer for guidance on safe disposal or alternatives.
Check for the lot number 36-260049 and expiration date 10/3/2023 on the IV bag. The product is labeled as epinephrine 2 mg added to dextrose 5% 250mL, concentration 8 mcg/mL, and is for prescription use only.
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-1129-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1129-2023 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.
