Central Admixture Pharmacy Services recalls specific Cardioplegia Solution batches due to potential contamination. Products intended to be sterile may not meet sterility standards after FDA inspection.
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 is recalling certain Cardioplegia Solution products because an FDA inspection raised concerns about their sterility. This could lead to infections if used in medical procedures.
The products were intended to be sterile but an FDA inspection found potential contamination. This could cause infections in patients during medical procedures if the solution is not properly sterile.
Healthcare professionals who use these products in medical procedures are most at risk. Patients receiving the solution during surgery may be affected if the product is contaminated.
Check for lot numbers 37-895694, 37-896050, 37-898304, 37-899234, or 37-901375 with expiration dates up to May 2023. The product is a sterile Cardioplegia Solution used for medical procedures.
Look for lot numbers 37-895694, 37-896050, 37-898304, 37-899234, or 37-901375 on the packaging.
The FDA inspection raised concerns about sterility, so these specific batches should not be used until recalled.
Check the lot numbers on the packaging: 37-895694, 37-896050, 37-898304, 37-899234, or 37-901375 with expiration dates up to May 2023.
The recall does not specify a remedy, so contact the manufacturer for guidance on safe disposal or alternatives.
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-0679-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0679-2023 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.
