Central Admixture Pharmacy Services recalls fentanyl syringes due to lack of sterility assurance. This may cause infections if used improperly. Affected products have specific lot numbers and expiration dates.
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 sterility assurance, which could lead to infections if the syringes are used without proper cleaning.
The syringes were repackaged by Central Admixture Pharmacy Services without sufficient sterility assurance. This means the syringes might not be clean enough to prevent infections when used for medical injections.
Patients prescribed fentanyl injections by a doctor who received the recalled syringes from Central Admixture Pharmacy Services. Healthcare providers using these syringes for medical purposes are also at risk.
Check for the lot numbers 17-275479 (expiring 10/4/2023) or 17-275852 (expiring 10/11/2023) on the syringe packaging. The product is a fentanyl syringe labeled as 250 mcg/5 mL, repackaged by CAPS Inc.
Look for lot numbers 17-275479 or 17-275852 on the syringe packaging.
The recall is due to a lack of sterility assurance, which could lead to infections if the syringes are used without proper cleaning.
The official notice does not specify a remedy, so check with your healthcare provider or pharmacy for guidance.
Check for lot numbers 17-275479 (expiring 10/4/2023) or 17-275852 (expiring 10/11/2023) on the syringe packaging.
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-0020-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0020-2024 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.
