Tailor Made Compounding recalls testosterone cypionate vials due to lack of sterility assurance. Affected batches expired by 2022-08-29. No remedy specified in official notice.
Lack of Assurance of Sterility
Tailor Made Compounding has recalled testosterone cypionate vials (1mL and 2mL) that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches with expiration dates up to August 2022.
The vials lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If injected, this could cause infections or other health issues. The product is intended for medical use, so improper sterility poses a serious health risk.
People who purchased the recalled testosterone cypionate vials from Tailor Made Compounding between 2021 and 2022 are affected. Those using the product for medical purposes without proper sterility checks are at higher risk.
Check for vial labels with batch numbers: 12212109A2, 01312217A1, 10202108A1, 12012125A, 02182230A1, or 03022222A1. The vials were sold at room temperature and expired by August 2022.
Look for specific batch numbers listed in the recall notice to identify affected vials.
The product lacks assurance of sterility, which could lead to infections if used improperly.
Batches with specific batch numbers: 12212109A2, 01312217A1, 10202108A1, 12012125A, 02182230A1, and 03022222A1.
The official notice does not specify a remedy, so no action is required beyond checking the batch numbers.
We’ve drafted a message you can send Tailor Made Compounding to request your refund or repair — edit it as you like.
Subject: Recall D-1230-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1230-2022 from Tailor Made Compounding. 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.
