Central Admixture Pharmacy Services recalls phenylephrine IV bags (NDC 72196-6058-1) with lot numbers 36-260033 and 36-260034 due to insufficient sanitization validation. These bags are for IV use only and may not be sterile, posing a risk of infection.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services has recalled phenylephrine IV bags that were prepared for hospital use. The bags lack proper sterility validation, which could lead to infections if used in medical procedures.
The bags were not properly validated for sanitization cycles, meaning they may not be sterile. This lack of sterility could cause infections in patients during medical procedures.
Healthcare facilities using these specific IV bags for patient treatment are affected. Patients receiving IV medication from these bags could be at risk of infection.
Check for the product name 'PHENYLephrine' in 0.9% sodium chloride, 10mg/250ml (40mcg/mL) IV bags. Look for lot numbers 36-260033 or 36-260034 with expiration date 10/3/2023.
Look for lot numbers 36-260033 or 36-260034 on the IV bag label.
Reach out to Central Admixture Pharmacy Services at 2200 South 43rd Avenue, Phoenix, AZ 85043 for further assistance.
The recall indicates a lack of sterility validation, so these bags may not be safe for medical use. Do not use them.
Check the lot number on the bag. If it matches 36-260033 or 36-260034, contact Central Admixture Pharmacy Services for instructions.
Look for the lot numbers 36-260033 or 36-260034 on the IV bag label with expiration date 10/3/2023.
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-1125-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1125-2023 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.
