Central Admixture Pharmacy Services recalls specific vasopressin solutions for potential lack of sterility after FDA inspection. These products are for medical use only and require immediate attention.
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 vasopressin solutions that may not be sterile. This risk could lead to infections if used in medical procedures.
The FDA inspection raised concerns about the sterility of these products. If not properly sterile, the vasopressin solutions could cause infections when used in medical procedures.
Healthcare professionals and patients receiving vasopressin treatments through these specific pharmacy products. Those using the recalled products are at risk of infection.
Check for lot numbers 37-886252, 37-886254, 37-889741, 37-889746, 37-891444, 37-893155, 37-893156, or 37-896812. The products expire by May 2023, June 2023, or July 2023.
Identify the lot numbers on the product label to determine if it is recalled.
The FDA has raised concerns about sterility, so these products should not be used until recalled.
The recall does not specify a remedy, so contact the manufacturer for guidance.
Check the lot numbers listed in the recall notice: 37-886252, 37-886254, 37-889741, 37-889746, 37-891444, 37-893155, 37-893156, or 37-896812.
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-0747-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0747-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.