ProRx recalls Semag: 2.5mg/1mL injections due to lack of sterility assurance. Affected units may cause infection if used. Return to pharmacy for replacement.
Lack of Assurance of Sterility
ProRx is recalling 2.5mg/1mL Semaglutide injections because they may not be sterile, which could lead to infections. This is serious for people using the product for weight loss.
The injections may not be sterile, meaning they could cause infections when injected. This is a serious risk for people using the product for weight loss.
People with prescriptions for Semaglutide injections from ProRx are affected. Those using the product for weight loss are at highest risk.
Check for the product name 'Semaglutide Injection, 2.5mg/1mL (2.5 mg/mL), 1mL Multidose Vial' on the label. The manufacturer is ProRx LLC, and the NDC code is 84139-225-06.
Immediately stop using the recalled Semaglutide injections as they may not be sterile and could cause infections.
No, the product may not be sterile and could cause infections. Do not use it.
Check for the product name 'Semaglutide Injection, 2.5mg/1mL (2.5 mg/mL), 1mL Multidose Vial' on the label. The manufacturer is ProRx LLC, and the NDC code is 84139-225-06.
Stop using it immediately and contact your pharmacy for a replacement.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0118-2026 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0118-2026 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.
