Tailor Made Compounding recalls testosterone vials due to lack of sterility assurance. Affected batches expired by 2022-07-13. Consumers should contact for details.
Lack of Assurance of Sterility
Tailor Made Compounding has recalled testosterone vials that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches with expiration dates up to July 2022.
The vials lack proper sterility assurance, which means they could be contaminated with bacteria. If used without proper sterilization, this could cause infections or other health issues.
Individuals who purchased the recalled testosterone vials from Tailor Made Compounding between 2021 and 2022 are affected. Those using the product for medical purposes are at higher risk due to potential infection.
Check for batch numbers: 11042102A1 (exp 4/30/2022), 12072135A1 (exp 6/5/2022), 01142228A1 (exp 7/13/2022), or 02182231A1 (exp 8/17/2022). The product was sold at room temperature.
Look for batch numbers on the vial: 11042102A1, 12072135A1, 01142228A1, or 02182231A1.
The recall states there is a lack of sterility assurance, so these vials may not be safe to use and could cause infections.
The official recall does not specify a remedy, so contact Tailor Made Compounding directly for instructions.
Check the batch numbers listed: 11042102A1 (exp 4/30/2022), 12072135A1 (exp 6/5/2022), 01142228A1 (exp 7/13/2022), or 02182231A1 (exp 8/17/2022).
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-1236-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1236-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
