Central Admixture Pharmacy Services recalls specific lots of Cardioplegia Solution due to potential contamination. This sterile product, used in cardiac surgery, may not be sterile after FDA inspection. Affected lots expire by April 2023.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services recalls certain lots of Cardioplegia Solution for cardiac surgery. The products may not be sterile after an FDA inspection, which could lead to infections if used in medical procedures.
The FDA inspection found the products might not be sterile. Cardioplegia Solution is used during heart surgery to protect the heart. If contaminated, it could cause infections in patients.
Healthcare professionals using this product for cardiac surgery. Patients undergoing heart procedures are at risk if the solution is contaminated.
Check for lot numbers 37-894307, 37-896158, 37-898281, or 37-900321. These lots expire by April 2023, May 2023, May 2023, or May 2023 respectively.
Look for lot numbers 37-894307, 37-896158, 37-898281, or 37-900321 on the packaging.
The FDA inspection raised concerns about sterility, but the product is still being used. It may not be sterile, which could lead to infections during surgery.
Check the lot number on the packaging. The recalled lots are 37-894307, 37-896158, 37-898281, or 37-900321.
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-0664-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0664-2023 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.
