Central Admixture Pharmacy Services recalls vancomycin solutions due to potential contamination. Products may not be sterile after FDA inspection. Affected lots expire May 2023. Contact for details.
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 recalled vancomycin solutions that may not be sterile after an FDA inspection. This could lead to infections if used in medical treatments. Patients using these products should stop using them immediately.
The FDA inspection found the products may not be sterile. Vancomycin is a critical antibiotic used in medical settings. If the solution is contaminated, it could cause serious infections in patients during treatment.
Healthcare facilities and medical professionals who use these vancomycin solutions for patient treatment. Patients receiving these medications through hospital or clinic administration are most at risk.
Check for the lot numbers listed (e.g., 37-883407) and expiration dates (May 2023). The product is a 250 mL bag of vancomycin added to 0.9% sodium chloride, labeled as Rx only for central pharmacy use.
Discontinue use of the recalled vancomycin solutions as they may not be sterile and could cause infections.
The product is vancomycin added to 0.9% sodium chloride, 1.25 g/250 mL (5 mg/mL), sold in 250 mL bags for medical use only.
Affected lots include 37-883407, 37-883436, 37-883796, and others listed in the recall notice with expiration dates through May 2023.
Check the lot number on the product label; affected lots are listed in the recall notice with specific expiration dates through May 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-0720-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0720-2023 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.
