Tailor Made Compounding recalls PT-141 10mg/mL vials due to lack of sterility assurance. Affected batches expire by April 2022. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
Tailor Made Compounding has recalled specific batches of PT-141 10mg/mL vials because they may not be sterile. This could lead to infections if used improperly. Affected customers should check their batch numbers and contact the company for instructions.
The vials may not be sterile, which can cause infections if the medication is used. This is a serious risk for individuals who require the medication for medical treatments.
People who have purchased PT-141 10mg/mL vials from Tailor Made Compounding are affected. Those using the product for medical purposes are at higher risk due to potential contamination.
Check the batch number on the vial label. Affected batches include 01042226A2 (exp 4/4/2022), 01242228A2 (exp 4/24/2022), and others listed in the recall notice.
Look for the batch number on the vial label to determine if it is affected.
Affected batches include 01042226A2 (exp 4/4/2022), 01242228A2 (exp 4/24/2022), 02212208A1 (exp 5/22/2022), and others listed in the recall notice.
Check the batch number on the vial label. The affected batches are listed in the recall notice.
Contact Tailor Made Compounding directly for instructions on what to do with the product.
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-1223-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1223-2022 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.
