Central Admixture Pharmacy Services recalls specific sterile IV solutions after FDA inspection raised sterility concerns. Products may not be sterile, posing infection risks. Check NDC 71285-8029-1 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 certain sterile IV solutions due to FDA concerns about their sterility. Using these products could lead to infections if not properly sterilized.
The FDA inspection found potential issues with the sterility of the products. This means the solutions might not be sterile when used, which could cause infections in patients.
Healthcare facilities and patients receiving these sterile IV solutions through prescription. Those using the recalled products are at risk of infection.
Check for NDC 71285-8029-1 and lot numbers: 37-882955 (exp 04/29/2023), 37-884753/37-884755 (exp 05/06/2023), 37-887536/37-887537 (exp 05/17/2023), 37-888532 (exp 05/23/2023), 37-892474 (exp 06/07/2023), 37-896761 (exp 06/23/2023), and 37-897261 (exp 06/27/2023).
Look for NDC 71285-8029-1 and the listed lot numbers to confirm if your product is affected.
The FDA inspection raised concerns about the sterility of these products, which could lead to infections if used.
Check for NDC 71285-8029-1 and the specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact the manufacturer for guidance.
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-0750-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0750-2023 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.
