ProRx recalls compounded Tirzepatide injections due to lack of sterility assurance. Affected vials may cause infections if used. Contact ProRx for details.
Lack of Assurance of Sterility
ProRx is recalling compounded Tirzepatide injections because they lack sterility assurance. Using these vials could lead to infections if they are not properly sterilized.
The vials lack proper sterility assurance, meaning they could become contaminated during manufacturing or storage. This contamination risk could lead to infections if the vials are used without proper sterilization.
People who have been prescribed compounded Tirzepatide injections by a healthcare provider. Those using the vials for medical treatment are most at risk.
Check for vials labeled 'Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection' compounded by ProRx. The lot number is ProRx040924-1 with a best use date of 10/08/2024.
Look for the product name and lot number on the vial to confirm it matches the recalled items.
The vials lack assurance of sterility, which could lead to infections if used without proper sterilization.
Check for vials labeled 'Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection' compounded by ProRx with lot number ProRx040924-1.
The recall record does not specify a remedy, so contact ProRx directly for guidance.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0651-2024 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0651-2024 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.
