Central Admixture Pharmacy Services recalls Cardioplegia Solution IV bags (NDC 72196-0216-1) with potential sterility issues. This recall affects specific lots manufactured in 2023.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution IV bags that may not be sterile. This could lead to infections if used in medical procedures. The recall is for specific lots produced in 2023.
The solution may not be sterile due to insufficient validation data for decontamination cycles. This could lead to infections if the product is used in medical procedures.
Healthcare professionals using these IV bags for medical procedures are affected. Patients receiving the solution through these bags are at risk of infection.
Check for the NDC number 72196-0216-1 and lot number 36-257024 on the IV bag. The product was manufactured in 2023 and expires August 14, 2023.
Look for the NDC number 72196-0216-1 and lot number 36-257024 on the IV bag.
The recall states there is a lack of assurance of sterility, so it is not safe to use.
The recall does not specify a remedy, so contact the manufacturer for guidance.
The product was manufactured in 2023 with an expiration date of August 14, 2023.
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-1015-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1015-2023 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.