Central Admixture Pharmacy Services recalls high-potassium cardioplegia solution due to lack of sterility assurance. Affected units have specific NDC and expiration dates. Consumers should contact the manufacturer for details.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling high-potassium cardioplegia solution IV bags because they may not be sterile. This could lead to infections if used in medical procedures.
The solution may not be sterile due to insufficient validation data for decontamination cycles. This could lead to infections if the product is used in medical procedures without proper sterility assurance.
Healthcare professionals using the recalled cardioplegia solution for medical procedures are most at risk. Patients receiving the solution could be affected if the product is used without proper sterility.
Check for NDC number 72196-0100-1 and lot numbers 36-251685 (expiring 7/15/2023) or 36-252364 (expiring 7/17/2023). The product is a high-potassium IV bag used in central admixture pharmacy services.
Reach out to Central Admixture Pharmacy Services at 2200 South 43rd Avenue, Phoenix, AZ 85043 for specific recall details.
The recall indicates a lack of sterility assurance, so it is not safe for medical use without proper validation.
Contact Central Admixture Pharmacy Services for specific instructions on handling the recalled product.
Look for NDC number 72196-0100-1 and lot numbers 36-251685 (expiring 7/15/2023) or 36-252364 (expiring 7/17/2023).
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-1028-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1028-2023 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.
