ProRx recalls TIRZEPATIDE 60mg/3mL vials due to lack of sterility assurance. Affected vials have specific lot numbers and expiration dates. Consumers should contact ProRx for details.
Lack of Assurance of Sterility
ProRx is recalling TIRZEPATIDE 60 mg/3mL vials because they may not be sterile. This could lead to infections if the medication is used. The recall affects specific lot numbers with expiration dates.
The vials lack assurance of sterility, meaning they might contain harmful bacteria. If the medication is injected, this could cause infections or other health issues. The hazard is not described in detail enough to determine exact risk levels.
Prescription users of TIRZEPATIDE 60 mg/3mL vials from ProRx. Those with specific lot numbers (ProRx052224 or ProRx061024) are most at risk.
Check the vial label for lot numbers: ProRx052224 (BUD 11/21/2024) or ProRx061024 (BUD 12/09/2024). The product is a prescription-only TIRZEPATIDE 60 mg/3mL vial.
Look for lot numbers on the vial: ProRx052224 or ProRx061024.
TIRZEPATIDE 60 mg/3mL (20/mg/mL) prescription vials with lot numbers ProRx052224 or ProRx061024.
Check the vial label for lot numbers: ProRx052224 (BUD 11/21/2024) or ProRx061024 (BUD 12/09/2024).
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-0656-2024 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0656-2024 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.
