Tailor Made Compounding recalls specific batches of Glutathione 200mg/ml vials due to lack of sterility assurance. Consumers should check batch numbers and contact the company for details.
Lack of Assurance of Sterility
Tailor Made Compounding has recalled certain batches of Glutathione 200mg/ml vials because they may not be sterile. This could pose a risk of infection if used improperly.
The vials may not be sterile, which could lead to infections if the product is used without proper hygiene. This is a serious concern for medical use.
People who purchased the recalled Glutathione 200mg/ml vials from Tailor Made Compounding are affected. Those using the product for medical purposes are at higher risk.
Check the batch numbers listed in the recall notice: 01122204A1, 02192214A1, 12142122A2, 12282118A2, 01112203A1, 01122208A1, 01202211A2, 02032205A1, 02192212A1, 03042201A1.
Look for batch numbers on the vial: 01122204A1, 02192214A1, 12142122A2, 12282118A2, 01112203A1, 01122208A1, 01202211A2, 02032205A1, 02192212A1, or 03042201A1.
The recalled batches have specific batch numbers: 01122204A1, 02192214A1, 12142122A2, 12282118A2, 01112203A1, 01122208A1, 01202211A2, 02032205A1, 02192212A1, and 03042201A1.
Check the batch number on the vial against the list provided in the recall notice.
The recall does not specify a remedy, so contact Tailor Made Compounding directly for further instructions.
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-1243-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1243-2022 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.
