Central Admixture Pharmacy Services recalls phenylephrine syringes (NDC 71286-6009-1) with specific lot numbers due to lack of sterility assurance from sanitization cycles. This affects central pharmacy use only.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling phenylephrine syringes that may not be sterile due to insufficient validation of sanitization cycles. This poses a risk of infection for patients receiving these medications through central pharmacy services.
The syringes lack proper validation data for their sanitization cycles, meaning they may not be sterile. This could lead to infections if the medication is administered to patients through these syringes.
Healthcare professionals using central pharmacy services for medication preparation are most at risk. Patients receiving these medications through central pharmacy services could be affected if the syringes are used improperly.
Check for lot numbers 17-270449 through 17-273965 on the syringe packaging. These syringes were sold to central pharmacies between August 2023 and September 2023.
Look for lot numbers 17-270449 through 17-273965 on the syringe packaging.
The recall states there is a lack of assurance of sterility due to insufficient validation of sanitization cycles, so it is not safe to use.
Check for lot numbers 17-270449 through 17-273965 on the syringe packaging. These syringes were sold to central pharmacies between August 2023 and September 2023.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
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-1066-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1066-2023 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.
