Central Admixture Pharmacy Services recalls potassium phosphate 15 mmole IV bags due to lack of sterility assurance. These bags may cause infections if used in medical procedures.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling potassium phosphate 15 mmole IV bags that were added to 0.9% sodium chloride. The bags lack proper sterility assurance, which could lead to infections if used in medical procedures.
The recall states that validation data for decontamination cycles is lacking, meaning the bags may not be sterile. This could lead to infections if used in medical procedures where sterility is critical.
Healthcare professionals using these IV bags for medical treatments. Patients receiving IV therapy with these specific bags are at risk of infection.
Check for the NDC number 72196-6060-1 and lot numbers listed in the recall (e.g., 36-239332 to 36-255879). These bags were sold with expiration dates from July 2023 through September 2023.
Look for the NDC number 72196-6060-1 and lot numbers listed in the recall (e.g., 36-239332 to 36-255879).
The recall is due to a lack of assurance of sterility, as validation data for decontamination cycles is lacking.
The official notice does not specify a remedy, so check with your healthcare provider or pharmacy for guidance.
Yes, the products have expiration dates from July 2023 through September 2023, 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-0989-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0989-2023 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.
