Central Admixture Pharmacy Services recalls fentanyl syringes due to lack of sterility assurance. These syringes may cause infections if used improperly. Contact the manufacturer for details.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl syringes that may not be sterile, posing infection risks. This recall affects medical use only and requires immediate attention from healthcare providers.
The syringes lack proper sterility assurance, meaning they could become contaminated during manufacturing or handling. This contamination risk increases the chance of infections when used for medical injections.
Healthcare providers and medical facilities using these fentanyl syringes are most at risk. Patients receiving fentanyl injections through these syringes could face infection.
Check for the NDC code 71286-2071-1 and lot numbers 17-275621, 17-275693, or 17-275725. These syringes were sold with expiration dates of October 8, 2023, or October 9, 2023.
Verify the NDC code 71286-2071-1 and lot numbers 17-275621, 17-275693, or 17-275725 to confirm if your syringe is affected.
The recall is due to a lack of assurance of sterility, which could lead to infections if the syringe is used improperly.
The official recall notice does not specify a remedy, so contact Central Admixture Pharmacy Services directly 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-0009-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0009-2024 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.
