Central Admixture Pharmacy Services recalls DilTIAZem added to 0.9% sodium chloride due to potential lack of sterility after FDA inspection. Affected lots expire by June 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 recalls specific DilTIAZem solutions for sterile use because an FDA inspection raised concerns about sterility. These products are for hospital use only and must be discarded if they match the listed lot numbers.
The FDA inspection found potential lack of sterility in these products, which are meant to be sterile. If the solutions were contaminated, they could cause infections in patients during intravenous administration.
Healthcare facilities using these DilTIAZem solutions for sterile intravenous administration are affected. Patients receiving these products could face infection risks if the solutions were not properly sterile.
Check the lot numbers listed: 37-896374, 37-896375, 37-896876, 37-896878, 37-897077, 37-897078, 37-900074, 37-900075, 37-900076, 37-900111, 37-900112, 37-900115, 37-900328. Products expire by May 31, 2023 through June 16, 2023.
Immediately discard any DilTIAZem solutions with the listed lot numbers as they may not be sterile.
An FDA inspection raised concerns about the sterility of these DilTIAZem solutions, which are meant to be sterile for intravenous use.
Affected lot numbers include 37-896374, 37-896375, 37-896876, 37-896878, 37-897077, 37-897078, 37-900074, 37-900075, 37-900076, 37-900111, 37-900112, 37-900115, and 37-900328.
Check the lot numbers on the product packaging; affected lots expire by May 31, 2023 through June 16, 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-0713-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0713-2023 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.
