Central Admixture Pharmacy Services recalls phenylephrine solution for potential contamination. Products may not be sterile, posing infection risks. Check NDC 71285-6092-1 and lot numbers for affected items.
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 phenylephrine solution products due to concerns about sterility after an FDA inspection. These products, used in medical settings, could cause infections if not properly sterile.
The FDA inspection found potential contamination in the products intended to be sterile. This lack of sterility could lead to infections in patients during medical procedures if the solution is not properly sterile.
Healthcare professionals and facilities using these products for medical injections. Patients receiving treatments with the recalled solution are at risk of infection.
Check for NDC 71285-6092-1 and lot numbers listed: 37-883910 through 37-898558. Products were sold between 2022 and 2023 with expiration dates up to May 2023.
Verify the NDC code 71285-6092-1 and lot numbers listed in the recall notice to confirm if your product is affected.
The FDA inspection raised concerns about the sterility of these phenylephrine solutions, which could lead to infections if used in medical procedures.
Check the NDC code and lot numbers listed in the recall notice to determine if your product is affected. If it is, contact the manufacturer for guidance.
Yes, the lack of sterility could cause infections in patients during medical procedures, so affected products should not be used.
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-0724-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0724-2023 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.
