Central Admixture Pharmacy Services recalls Cardioplegia Solution IV bags (NDC 72196-0218-1) 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 IV bags due to a lack of assurance of sterility. This could lead to contamination during medical use, posing a risk to patients receiving the solution.
The product lacks validation data for decontamination cycles, meaning it may not be sterile when prepared for medical use. This could lead to contamination during IV administration, potentially causing infections or other complications in patients.
Healthcare professionals using the recalled Cardioplegia Solution for medical procedures are most at risk. Patients receiving the solution through IV administration may be affected if the product is used without proper sterility.
Check for the NDC code 72196-0218-1 on the product label. The product was manufactured in Lot 36-255941 and expires July 27, 2023.
Look for the NDC code 72196-0218-1 and lot number 36-255941 on the IV bag.
The official recall notice states that validation data for decontamination cycles is lacking, so the product may not be sterile and is not safe for medical use.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance on next steps.
Check the NDC code 72196-0218-1 and lot number 36-255941 on the product 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-1025-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1025-2023 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.
