Central Admixture Pharmacy Services recalls potassium phosphate IV bags due to lack of sterility assurance. This affects specific lots manufactured in Phoenix, AZ. Patients using these bags for IV treatments may face infection risks.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling potassium phosphate IV bags that were added to 0.9% sodium chloride solution. The bags lack proper sterility assurance, which could lead to infections if used in medical treatments.
The product lacks validation data for decontamination cycles, meaning it may not be sterile when used. This could lead to infections in patients receiving intravenous treatments.
Healthcare professionals using these IV bags for patient treatments in hospitals or clinics. Patients receiving IV therapy with this specific product are at risk of infection.
Check for the product name: potassium phosphate, 30 mmole added to 0.9% sodium chloride 500mL IV bag. The lot number 36-256240 and expiration date 9/12/2023 are specific to this recall.
Identify the lot number and expiration date on the IV bag to confirm if it matches the recalled batch.
The recall indicates a lack of sterility assurance, so it is not safe for medical use. Patients should not use this product without contacting the manufacturer.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance on safe disposal or alternatives.
Check the lot number and expiration date on the IV bag; the recalled product has lot 36-256240 and expires 9/12/2023.
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-0990-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0990-2023 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.
