Central Admixture Pharmacy Services recalls PHENYLephrine 20mg/250ml IV bags due to lack of sterility validation. Affected lots expire through August 2023. No remedy specified in recall notice.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling certain PHENYLephrine 20mg/250ml IV bags because they lack proper sterility validation. This could lead to infections if used in medical procedures.
The bags were manufactured without sufficient validation data to ensure they remain sterile during decontamination cycles. This means the solution could become contaminated, potentially causing infections in patients during medical procedures.
Healthcare professionals using these IV bags for medical treatments. Patients receiving injections from these bags are at risk of infection.
Check for lot numbers 36-239194 through 36-251966 on the IV bag packaging. These products were sold with expiration dates from July 10, 2023, through August 30, 2023.
Look for lot numbers 36-239194 through 36-251966 on the IV bag packaging.
The recall is due to lack of assurance of sterility. Validation data for decontamination cycles is lacking, which could lead to contamination.
The recall notice does not specify a remedy. Check the lot number to see if your product is affected.
Yes, the product could become contaminated, leading to infections if used in medical procedures.
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-0961-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0961-2023 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.
