Tailor Made Compounding recalls specific GAC vials due to lack of sterility assurance. Affected batches expire by March 2022. Consumers should check batch numbers on vials.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling certain GAC (Glutamine/Arginine/L-Carnitine) vials because they may not be sterile. This could lead to infections if used improperly.
The vials may not be sterile, which could cause infections if the product is used without proper hygiene. This is a serious health risk for individuals with compromised immune systems or those using the product for medical treatments.
People who have the specific GAC vials with batch numbers listed in the recall are affected. Those using the product for medical purposes are at higher risk.
Check the vial label for batch numbers: 10122110A2 (exp 3/20/2022), 12062110A2 (exp 4/30/2022), 02012202A2, or 02192207A1 (exp 7/31/2022).
Look for batch numbers on the vial label: 10122110A2, 12062110A2, 02012202A2, or 02192207A1.
GAC (Glutamine/Arginine/L-Carnitine) 25mg/100mg/250mg/mL vials with specific batch numbers.
Check the vial label for batch numbers: 10122110A2 (exp 3/20/2022), 12062110A2 (exp 4/30/2022), 02012202A2, or 02192207A1 (exp 7/31/2022).
The recall does not specify a remedy, so contact the manufacturer for guidance.
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-1203-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1203-2022 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.
