Central Admixture Pharmacy Services recalls Cardioplegia Solution del Nido Formula IV bags due to lack of sterility assurance. Products with specific NDC and expiration dates are affected.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution del Nido Formula IV bags because they lack proper sterility assurance. This could lead to infections if used in cardiac procedures, so affected users should stop using the product immediately.
The solution lacks validation data for decontamination cycles, meaning it may not be sterile. This could cause infections during cardiac procedures if the product is used without proper sterility.
Healthcare professionals using this solution for intracardiac perfusion are affected. Patients undergoing cardiac surgery who received this product are at risk of infection.
Check for the NDC number 72196-0202-1 and expiration dates listed in the recall (e.g., 8/1/2023, 8/5/2023). The product is for intracardiac perfusion only and requires a prescription.
Discard the product if you have it, as it may not be sterile and could cause infections during cardiac procedures.
No, the product lacks sterility assurance and could cause infections during cardiac procedures. Do not use it.
The NDC number is 72196-0202-1.
Expire dates include 7/10/2023, 8/1/2023, 8/5/2023, 8/7/2023, 8/8/2023, 8/11/2023, and others as listed in the recall.
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-0956-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0956-2023 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.
