ProRx recalls Semaglutide/Cyanocobalamin injection vials with potential contamination. Affected vials have NDC 84139-225-02 and Lot # ProRx031924-1. Consumers should contact ProRx for details.
Lack of Assurance of Sterility
ProRx is recalling a compounded semaglutide injection product due to a lack of assurance of sterility. This means the product could be contaminated, which poses a risk of infection or other health issues if used.
The product lacks assurance of sterility, meaning it may contain harmful bacteria or other contaminants. If the injection is used without proper sterility, it could lead to infections or other health complications.
People who have received this compounded injection product from a healthcare provider. Those using the product for weight management or diabetes treatment are most at risk.
Check for the NDC code 84139-225-02 and lot number ProRx031924-1 on the vial label. This compounded injection was sold through healthcare providers starting in 2024.
Reach out to ProRx at 267-565-7008 for specific instructions on handling the recalled product.
The recall states there is a lack of assurance of sterility, so it is not safe to use without contacting ProRx first.
Contact ProRx at 267-565-7008 for specific instructions on handling the recalled product.
Look for the NDC code 84139-225-02 and lot number ProRx031924-1 on the vial label.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0654-2024 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0654-2024 from ProRx. 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.
