ProRx recalls compounded SEMAGLUTIDE 10mg/4mL vials due to lack of sterility assurance. Affected units have NDC 84139-225-04 and were compounded by ProRx in Exton, PA. No remedy specified in recall notice.
Lack of Assurance of Sterility
ProRx is recalling compounded SEMAGLUTIDE 10mg/4mL vials because they lack sterility assurance. This means the medication could be contaminated, posing a risk of infection or illness if used.
The vial lacks proper sterility assurance, meaning it could be contaminated with bacteria or other pathogens. If the medication is injected, this contamination could cause infections or serious health issues.
People who have been prescribed this compounded medication by a doctor. Those using the vial for weight management treatment are most at risk.
Check for the NDC code 84139-225-04 on the vial label. The vial was compounded by ProRx in Exton, PA with a batch date of 12/13/2024.
Look for the NDC code 84139-225-04 on the vial label.
The recall states there is a lack of sterility assurance, so the medication may be contaminated. Do not use this vial.
The recall notice does not specify a remedy, so contact your doctor or pharmacist for guidance.
Check for the NDC code 84139-225-04 on the vial label. The vial was compounded by ProRx in Exton, PA with a batch date of 12/13/2024.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0653-2024 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0653-2024 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.
