Central Admixture Pharmacy Services recalls epinephrine IV bags (NDC 72196-8093-1) with lot #36-260047 due to insufficient sanitization validation. This could lead to infections if used in medical procedures.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling a specific epinephrine IV bag product because the manufacturing process did not properly validate sterilization. This poses a risk of infection if the bag is used in medical procedures.
The product lacks validated sanitization cycles, meaning the bags might not be sterile. If used in medical procedures, this could introduce harmful bacteria, leading to infections in patients.
Healthcare professionals who use this specific epinephrine IV bag for medical treatments may be affected. Patients receiving this medication through IV administration are at risk if the product is used without proper sterility.
Check for the product name 'EPINEPHrine added to 0.9% sodium chloride, 4mg/250mL (16 mcg/mL), IV Bag' and the lot number 36-260047. The expiration date is October 3, 2023.
Verify the lot number and expiration date on the IV bag to confirm if it matches the recalled batch.
The official recall does not state whether the product is safe to use. The lack of validated sanitization cycles means there is a risk of infection if used in medical procedures.
The recall record does not specify a remedy, so there is no action required beyond checking the product details.
The recall record does not mention a replacement or remedy, so no replacement is provided.
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-1130-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1130-2023 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.
