Central Admixture Pharmacy Services recalls Cardioplegia Solution due to potential contamination. Products may not be sterile as found in FDA inspections. Affected lots expire May 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 Cardioplegia Solution for possible contamination. This sterile medical product could cause infections if used improperly. The recall affects specific lots with expiration dates in May 2023.
The FDA found the products may not be sterile. Cardioplegia Solution is used during heart surgery to protect the heart. Contamination could lead to infections or other complications.
Healthcare professionals using this product for cardiac surgery may be affected. Patients receiving the solution through central lines are at risk if the product is contaminated.
Check for lot numbers 37-895256 or 37-898816 on the packaging. Products expire by May 4, 2023 or May 18, 2023. The product is sold only by prescription for cardiac procedures.
Look for lot numbers 37-895256 or 37-898816 on the packaging.
The FDA has raised concerns about sterility, so the product may not be safe. Do not use until the recall is resolved.
Check the lot number on the packaging. If it matches 37-895256 or 37-898816, contact the manufacturer for instructions.
The products expire by May 4, 2023 or May 18, 2023. Do not use after the expiration date.
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-0680-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0680-2023 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.
