Central Admixture Pharmacy Services recalls fentanyl syringes due to lack of sterility validation in sanitization cycles. These are prescription-only syringes with specific lot numbers and expiration dates.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl syringes that may not be sterile due to insufficient validation of sanitization cycles. This could lead to infections if used improperly.
The syringes lack validated sanitization cycles, meaning they might not be sterile. If used without proper sterility, this could cause infections in patients receiving fentanyl injections.
Prescription patients receiving fentanyl injections from this pharmacy. Healthcare providers using these syringes for medical treatments are at risk.
Check for lot numbers 17-271144 through 17-272457 with expiration dates from July 2023 to August 2023. These are prescription-only fentanyl syringes sold by Central Admixture Pharmacy Services.
Verify the lot number and expiration date on the syringe to confirm if it's in the recalled range.
The official recall does not state if the product is safe to use; it indicates a lack of sterility validation.
The recall record does not specify a remedy, so no action is required based on this notice.
Check the lot number and expiration date on the syringe. Recalled lots are 17-271144 through 17-272457 with expiration dates from July 2023 to August 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-1042-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1042-2023 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.