Tailor Made Compounding recalls Sermorelin/Glycine 2000mcg/5mg/mL vials due to lack of sterility assurance. Affected batches expire by May 2022. Consumers should check batch numbers and contact the company for details.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling specific batches of Sermorelin/Glycine 2000mcg/5mg/mL vials because they may not be sterile. This could lead to infections if used improperly.
The vials may not be sterile, which can cause infections if injected. This is a serious risk for medical treatments that require clean products.
People who have purchased or are using the recalled Sermorelin/Glycine vials from Tailor Made Compounding. Those with medical conditions requiring these injections are at higher risk.
Check the batch number on the vial label. The affected batches include 11102107A2 (exp 4/9/2022), 02212229A1 (exp 5/22/2022), and others listed in the recall notice.
Look for the batch number on the vial label to determine if it's affected. Affected batches are listed in the recall notice.
Tailor Made Compounding is recalling specific batches of Sermorelin/Glycine 2000mcg/5mg/mL vials due to a lack of sterility assurance.
Check the batch number on the vial label. Affected batches include 11102107A2 (exp 4/9/2022), 02212229A1 (exp 5/22/2022), and others listed in the recall notice.
The recall notice does not specify a remedy. 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-1227-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1227-2022 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.
