Central Admixture Pharmacy Services recalls phenylephrine IV bags (NDC 72196-7025-1) with potential sterility issues. This is for medical use only, not for home patients.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling phenylephrine IV bags that may not be sterile. This could lead to infections if used in medical settings.
The bags lack validated sanitization cycles, meaning they might not be sterile. This could cause infections if used in medical procedures.
Healthcare professionals using these IV bags in hospitals or clinics. Patients receiving IV treatments through this product are at risk.
Check for the NDC number 72196-7025-1 on the bag. The product was manufactured with lot number 36-260037 and expires October 3, 2023.
Look for the NDC number 72196-7025-1 and lot number 36-260037 on the IV bag.
No, this is a prescription-only medical product for IV use in healthcare settings.
The recall does not specify a remedy, so contact the manufacturer for guidance.
Check the NDC number 72196-7025-1 and lot number 36-260037 on the IV bag.
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-1126-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1126-2023 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.
