Central Admixture Pharmacy Services recalls Cardioplegia Solution (15 mEq K, Reperfusate 4:1) due to lack of sterility assurance. This product is for prescription use only and may pose infection risks if not properly sterilized.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution (15 mEq K, Reperfusate 4:1, 500mL) because it lacks proper sterility assurance. This could lead to infections if used in medical procedures.
The product lacks validation data for decontamination cycles, meaning it may not be properly sterilized. This could lead to infections if used in medical procedures where sterility is critical.
Prescription patients receiving Cardioplegia Solution for medical procedures. Healthcare professionals handling the product are at risk of exposure to unsterile solutions.
Check for the NDC code 72196-0009-1 and lot number 36-254914 on the product label. The product expires July 22, 2023, and is only available by prescription.
Look for NDC code 72196-0009-1 and lot number 36-254914 on the product label.
The product lacks validation data for decontamination cycles, so it may not be properly sterilized. It is not safe for medical use without proper sterility assurance.
The recall does not specify a remedy, so check the product label for NDC code 72196-0009-1 and lot number 36-254914 to confirm if it is affected.
The recall does not mention a replacement or remedy, so contact the manufacturer directly for assistance.
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-1020-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1020-2023 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.
