ProRx recalls Semaglutide injections with potential lack of sterility assurance. Affected lots from May 2025 production. Consumers should contact ProRx for details.
Lack of Assurance of Sterility
ProRx is recalling Semaglutide injections due to a lack of sterility assurance. This could lead to infections if the product is not properly sterile. The recall affects specific production lots.
The product lacks assurance of sterility, meaning it might not be free from harmful bacteria. If the injection is not sterile, it could cause infections when injected into the body. This is a serious risk for users who require the medication.
People who have received the Semaglutide injection from ProRx with the specified lot numbers (Prorx051525-1 to Prorx051525-4) are affected. Those using the product for weight management are most at risk.
Check the lot numbers on the vial: Prorx051525-1, Prorx051525-2, Prorx051525-3, or Prorx051525-4. The product was manufactured by ProRx at 619 Jeffers Cir, Exton, PA 19341.
Look for the lot numbers Prorx051525-1 through Prorx051525-4 on the vial.
Semaglutide Injection, 8mg/3.2mL (2.5 mg/mL), 3.2mL Multidose Vial, For Subcutaneous Use, Rx Only.
Lot numbers Prorx051525-1, Prorx051525-2, Prorx051525-3, and Prorx051525-4.
Check the lot number on the vial; affected lots are Prorx051525-1 through Prorx051525-4.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0117-2026 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0117-2026 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.
