Central Admixture Pharmacy Services recalls Cardioplegia Solution IV bags (NDC 72196-0111-1) with potential sterility issues. This medication is for IV use only and may pose infection risks if not properly sterilized.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution IV bags (500 mL, high potassium) because they lack proper sterility assurance. This could lead to infections if used in medical procedures.
The product lacks validation data for decontamination cycles, meaning it may not be sterile. This could lead to infections if the medication is used in medical procedures without proper sterilization.
Healthcare professionals who use this medication for IV treatments may be affected. Patients receiving this medication through a hospital or clinic are at risk if the product is not properly sterilized.
Check for the NDC code 72196-0111-1 and lot number 36-254403 on the IV bag. This product was sold with an expiration date of July 21, 2023.
Look for the NDC code 72196-0111-1 and lot number 36-254403 on the IV bag.
The product lacks validation data for decontamination cycles, so it may not be sterile. Healthcare professionals should not use it without proper sterilization.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe handling.
The recall was issued by Central Admixture Pharmacy Services, Inc. for the specific lot number 36-254403 with an expiration date of July 21, 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-1027-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1027-2023 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.
