Central Admixture Pharmacy Services recalls phenylephrine syringes (NDC 72196-6009-1) with specific lot numbers due to lack of validation data for sanitization cycles, posing a sterility risk.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services has recalled phenylephrine syringes that may not be sterile due to insufficient validation of sanitization cycles. This could lead to infections if used improperly.
The syringes lack validated sanitization cycles, meaning they might not be sterile when used. This could lead to infections if the medication is injected into the body.
Healthcare professionals and patients who have received the recalled phenylephrine syringes with specific lot numbers and expiration dates listed in the recall notice.
Check the product label for lot numbers 36-262311 to 36-262742 and expiration dates of October 5, 2023, or October 11, 2023. The product is a phenylephrine syringe for prescription use.
Look for lot numbers 36-262311 to 36-262742 and expiration dates of October 5, 2023, or October 11, 2023.
The recall is due to a lack of validation data for sanitization cycles, which could mean the syringes are not sterile.
Check the product label for the specific lot numbers and expiration dates listed in the recall notice. If you have the recalled product, contact the manufacturer for further instructions.
The recall indicates a potential sterility risk, which could lead to infections if the medication is injected, but the remedy is not specified in the record.
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-1124-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1124-2023 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.
