Central Admixture Pharmacy Services recalls fentanyl syringes due to lack of sterility assurance. This affects repackaged products with specific NDC and lot numbers. Consumers should contact the manufacturer for details.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling fentanyl syringes that were repackaged by their company. The recall is due to a lack of assurance of sterility, which could lead to infections if the syringes are used.
The syringes were repackaged by Central Admixture Pharmacy Services without proper sterility assurance. This means the syringes could be contaminated, leading to infections if used for medical purposes.
Individuals who have the specific fentanyl syringes with NDC 71286-2003-1 and lot number 17-275284 are affected. Healthcare professionals using these syringes for medical purposes are at the highest risk.
Check for the NDC number 71286-2003-1 and lot number 17-275284 on the syringe packaging. These syringes were repackaged by Central Admixture Pharmacy Services, Inc. and sold in San Diego, California.
Look for the NDC number 71286-2003-1 and lot number 17-275284 on the syringe packaging.
The recalled product is fentanyl syringes with NDC 71286-2003-1 and lot number 17-275284, repackaged by Central Admixture Pharmacy Services, Inc.
Check for the NDC number 71286-2003-1 and lot number 17-275284 on the syringe packaging.
The recall record does not specify a remedy, so contact Central Admixture Pharmacy Services, Inc. for 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-0019-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0019-2024 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.
