Central Admixture Pharmacy Services recalls Cardioplegia Solution (108 mEq K, 500mL IV bag) because validation data for decontamination cycles is lacking, risking contamination.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution (108 mEq K, 500mL IV bag) due to lack of assurance of sterility. This could lead to infections if the solution is used in medical procedures.
The solution lacks validation data for decontamination cycles, meaning it may not be sterile. If contaminated, it could cause infections in patients during medical procedures.
Healthcare professionals using this IV solution for medical procedures are affected. Patients receiving the solution could be at risk of infection.
Check for the product name 'Cardioplegia Solution', 108 mEq K, 500mL IV bag, with NDC 72196-0102-1 and lot number 36-255940.
Identify the product by checking the NDC number 72196-0102-1 and lot number 36-255940 on the packaging.
The recall states there is a lack of assurance of sterility, so it is not safe to use without the remedy.
Look for the NDC number 72196-0102-1 and lot number 36-255940 on the packaging.
The recall does not specify a remedy, so contact the manufacturer for guidance.
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-1032-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1032-2023 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.