Central Admixture Pharmacy Services recalls vancomycin solution due to lack of validation data for sanitization cycles. This affects specific lot numbers and expiration dates. Contact for remedy details.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling vancomycin solutions that were added to 0.9% Sodium Chloride. The recall is due to a lack of validation data for sanitization cycles, which could risk contamination.
The product lacks validated sanitization cycles, meaning the solution might not be sterile. This could lead to infections if the medication is used without proper sterility assurance.
Healthcare professionals using this medication in central line therapy. Patients receiving the vancomycin solution through this specific product are at risk.
Check for lot numbers 36-262215 or 36-262216 on the 250mL Excel Bag. The expiration date is October 5, 2023. This product is for prescription use only in central pharmacy settings.
Look for lot numbers 36-262215 or 36-262216 on the 250mL Excel Bag.
The recall states there is a lack of validation data for sanitization cycles, which could risk contamination. Do not use this product until the manufacturer provides a remedy.
The recall record does not specify a remedy, so contact Central Admixture Pharmacy Services for instructions.
Check for lot numbers 36-262215 or 36-262216 on the 250mL Excel Bag. The expiration date is October 5, 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-1136-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1136-2023 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.
