ProRx recalls Semaglutide injections with potential contamination risk. Affected lots have specific batch numbers and expiration dates. Consumers should contact ProRx for details.
Lack of Assurance of Sterility
ProRx is recalling certain Semaglutide injections due to a lack of assurance of sterility. This means the product could be contaminated, posing a risk of infection after injection.
The product lacks assurance of sterility, meaning it could be contaminated with bacteria or other pathogens. If injected, this could lead to infections or other health issues.
People who have been prescribed Semaglutide injections by a doctor and received the recalled lots. Those with the specific batch numbers listed are most at risk.
Check the product label for the batch numbers: PRORX050925-1, PRORX051425-5, or PRORX051425-6. The expiration date (BUD) for these lots is November 4, 2025 or November 10, 2025.
Look for the batch numbers: PRORX050925-1, PRORX051425-5, or PRORX051425-6 on the vial.
ProRx is recalling Semaglutide injections with a lack of assurance of sterility, which could lead to contamination.
Check the vial label for batch numbers: PRORX050925-1, PRORX051425-5, or PRORX051425-6.
The recall record does not specify a remedy, so contact ProRx directly for instructions.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0115-2026 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0115-2026 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.
