Central Admixture Pharmacy Services recalls fentanyl 2 mcg/mL and bupivacaine 0.125% solutions with potential lack of sterility due to unvalidated sanitization cycles. Affected lots expire through September 2023.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl 2 mcg/mL and bupivacaine 0.125% solutions that may not be sterile due to unvalidated sanitization cycles. This could lead to infections if used in medical procedures.
The solutions lack validated sanitization cycles, meaning they may not be sterile when prepared. This could cause infections in patients during medical procedures if the medication is administered without proper sterility.
Healthcare providers using these specific medical solutions for procedures. Patients receiving these medications are at risk of infection if the solution is not properly sterile.
Check for the lot numbers listed: 17-270540 through 17-274414, expiring through September 2023. These are prescription-only solutions sold by Central Admixture Pharmacy Services, Inc.
Identify the lot number on the product label, which should be one of the listed numbers (17-270540 through 17-274414).
The recall indicates a potential lack of sterility, so it is not safe to use without confirming the product is not recalled.
The official notice does not specify a remedy, so contact the manufacturer directly for guidance.
Check the lot number on the product label against the list provided: 17-270540 through 17-274414, expiring through September 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-1072-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1072-2023 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.
