Central Admixture Pharmacy Services recalls vancomycin solutions due to potential contamination during manufacturing. Products may not be sterile, posing infection risks. Check NDC 71285-6176-1 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 recalls certain vancomycin solutions because an FDA inspection found possible contamination. These products are meant to be sterile but may not be, increasing infection risk for patients receiving them through intravenous administration.
The FDA inspection identified potential contamination in the sterile vancomycin solutions. If the solution is not sterile, it could introduce harmful bacteria into the patient's bloodstream during intravenous administration, leading to infections.
Healthcare facilities using these vancomycin solutions for intravenous administration are most at risk. Patients receiving the medication through IV lines could face infections if the solution is not sterile.
Check for NDC 71285-6176-1 and lot numbers listed: 37-883372, 37-883387, 37-883790, 37-884160, 37-885320, 37-885321, 37-885324, 37-885921, 37-885928, 37-885930, 37-886270, 37-887511, 37-887666, 37-887670, 37-888115, 37-888841, 37-889457, 37-889462, 37-892638, 37-892641, 37-892648, 37-894437, 37-894443, 37-894450, 37-895707, 37-895718, 37-895723, 37-896532, 37-896535, 37-898527. Products were sold from 2021 to 2023.
Identify if your vancomycin solution has a lot number listed in the recall (e.g., 37-883372, 37-883387).
If you have the recalled product, contact your healthcare provider to discuss potential risks and next steps.
An FDA inspection found potential contamination in the sterile vancomycin solutions, which could lead to infections if used improperly.
The product may not be sterile, increasing the risk of infection for patients receiving intravenous administration.
Check the lot numbers listed in the recall: 37-883372, 37-883387, 37-883790, 37-884160, 37-885320, 37-885321, 37-885324, 37-885921, 37-885928, 37-885930, 37-886270, 37-887511, 37-887666, 37-887670, 37-888115, 37-888841, 37-889457, 37-889462, 37-892638, 37-892641, 37-892648, 37-894437, 37-894443, 37-894450, 37-895707, 37-895718, 37-895723, 37-896532, 37-896535, 37-898527.
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-0725-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0725-2023 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.
