Central Admixture Pharmacy Services recalls fentanyl syringes due to lack of validation data for sanitization cycles. This may cause contamination. Affected products have specific NDC and expiration dates.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl syringes because they lack validation data for sanitization cycles, which could lead to contamination. This is a serious issue for medical use since fentanyl is a potent opioid.
The syringes were manufactured without validated sanitization cycles, meaning they might not be sterile. This could lead to contamination with harmful bacteria or other pathogens when used for medical purposes.
Healthcare professionals and patients using prescription fentanyl syringes from Central Admixture Pharmacy Services. Those with the specific NDC numbers and expiration dates listed are most at risk.
Check for the NDC number 71286-2003-7 and expiration dates listed in the recall (e.g., 7/18/2023 to 9/14/2023). The syringes are prescription-only fentanyl products.
Look for the NDC number 71286-2003-7 and expiration dates listed in the recall (e.g., 7/18/2023 to 9/14/2023).
The recall is due to lack of validation data for sanitization cycles, which could mean the syringes are not sterile.
Check the NDC number and expiration dates listed in the recall. If you have the affected products, contact Central Admixture Pharmacy Services for guidance.
The recall record does not specify a remedy, so contact the manufacturer directly for 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-1043-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1043-2023 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.
