Central Admixture Pharmacy Services recalls Sodium Phosphates Injection 4 mEq/3 mMol/mL, 500ml bags due to potential contamination. Products may not be sterile, posing infection risks. Check NDC 71285-8077-1 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 is recalling Sodium Phosphates Injection 4 mEq/3 mMol/mL, 500ml bags because an FDA inspection raised concerns about sterility. Using these products could lead to infections since they're intended to be sterile.
The products were found to lack assurance of sterility during an FDA inspection. This means they could contain contaminants that might cause infections when used in medical procedures.
Healthcare professionals who use these products for medical treatments. Patients receiving injections from facilities using the recalled products are at risk of infection.
Check for NDC 71285-8077-1 and lot numbers: 37-883239, 37-883240 (exp 05/01/2023), 37-884419, 37-884423 (exp 05/04/2023), and other listed lots with expiration dates through 06/28/2023.
Identify the NDC 71285-8077-1 and lot numbers from the list provided in the recall notice.
An FDA inspection raised concerns about the sterility of these products, which are intended to be sterile.
The recall notice does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
Yes, the recall includes specific lot numbers like 37-883239, 37-883240 (exp 05/01/2023), and others listed with expiration dates through 06/28/2023.
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-0751-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0751-2023 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.
