Central Admixture Pharmacy Services recalls vasopressin 40 units in 100mL bags (NDC 71285-9001-1) due to potential sterility issues found during FDA inspection. Affected lots expire May 2023.
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 is recalling vasopressin solutions that may not be sterile. This could lead to infections if used in medical treatments. Patients and healthcare providers should stop using these products immediately.
The FDA inspection found potential sterility issues in the products intended to be sterile. This means the solutions could become contaminated and cause infections if used in medical procedures.
Healthcare providers and patients using the recalled vasopressin solutions for medical treatments. Those with the specific lot numbers and expiration date are most at risk.
Check for the lot numbers 37-889738 or 37-889742 on the packaging. The products expire May 25, 2023, and are labeled as vasopressin 40 units in 100mL bags.
Discard the recalled vasopressin solutions with lot numbers 37-889738 or 37-889742.
Vasopressin 40 units added to 0.9% sodium chloride 100 mL per bag (Rx only).
Lot numbers 37-889738 and 37-889742.
The products expire May 25, 2023.
The recall record does not specify a remedy.
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-0748-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0748-2023 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.