Central Admixture Pharmacy Services recalls IV bags containing phenylephrine that may not be sterile due to insufficient sanitization validation. Affected units have NDC 72196-6092-1 and lot 36-260036. Stop using immediately.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling IV bags containing phenylephrine that may not be sterile because sanitization cycles weren't properly validated. This could lead to infections if used in medical procedures.
The IV bags were made without sufficient validation of their sanitization cycles, meaning they might not be sterile. If used in medical procedures, this could cause infections in patients.
Healthcare professionals using these IV bags for medical treatments. Patients receiving IV therapy with these bags are at risk of infection.
Check for the NDC number 72196-6092-1 and lot number 36-260036 on the IV bag label. These bags were sold for prescription use by Central Admixture Pharmacy Services in the U.S.
Discard the IV bag if you have it and contact the manufacturer for a replacement.
No, these IV bags may not be sterile and could cause infections if used in medical procedures.
Discard the IV bag immediately and contact Central Admixture Pharmacy Services for a replacement.
Look for the NDC number 72196-6092-1 and lot number 36-260036 on the IV bag label.
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-1127-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1127-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
