Central Admixture Pharmacy Services recalls sterile phenylephrine solutions due to potential contamination risks identified during FDA inspections. Affected lots expire by May 2023. Contact for details.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services has recalled certain phenylephrine solutions that were found to lack sterility assurance during FDA inspections. This could lead to infections if used in medical procedures.
The products were found to have potential contamination during FDA inspections, which could lead to infections if used in medical procedures. This is a lack of sterility assurance for products intended to be sterile.
Healthcare professionals using these solutions for medical procedures are most at risk. Patients receiving these solutions through central lines may be affected.
Check for lot numbers 37-884272 through 37-898324 on the packaging. These products expire by May 2023 and are labeled as phenylephrine added to 0.9% sodium chloride for central line use.
Look for lot numbers 37-884272 through 37-898324 on the packaging.
Phenylephrine added to 0.9% sodium chloride, 10 mg/250 mL (40 mcg/mL), 250 mL per bag, for central line use.
The FDA identified potential contamination risks during inspections, indicating a lack of sterility assurance for products intended to be sterile.
Check the lot number on the packaging; affected lots range from 37-884272 to 37-898324 and expire by May 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-0715-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0715-2023 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.
