Central Admixture Pharmacy Services recalls fentanyl syringes (NDC 71286-2003-7) with specific lot numbers due to lack of sterility assurance. This could lead to infections if used improperly.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl syringes that may not be sterile, posing a risk of infection. This recall affects healthcare facilities using these syringes for medical treatments.
The syringes lack assurance of sterility, meaning they could be contaminated with bacteria. If used for injections, this could lead to infections in patients. The risk is primarily for medical settings where the syringes are handled.
Healthcare facilities and medical professionals using these fentanyl syringes for patient treatments. Patients receiving injections with these syringes are at risk of infection.
Check for lot numbers 17-275223, 17-275275, 17-275928, 17-276088, or 17-276118 with expiration dates up to October 2023. These syringes are labeled as fentanyl 1,250 mcg/25 mL (50 mcg/mL) for prescription use.
Look for lot numbers 17-275223, 17-275275, 17-275928, 17-276088, or 17-276118 on the syringe packaging.
The recall is due to a lack of assurance of sterility, which could lead to infections if the syringes are used for injections.
The official notice does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
The recall indicates they may not be sterile, so they should not be used until the manufacturer provides further instructions.
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-0025-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0025-2024 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.
