Tailor Made Compounding recalls specific batches of Methionine/Inositol/Choline B12 vials due to lack of sterility assurance. Affected batches have expiration dates through June 2022. Consumers should check batch numbers and contact the manufacturer for details.
Lack of Assurance of Sterility
Tailor Made Compounding has recalled certain batches of Methionine/Inositol/Choline B12 vials because they may not be sterile. This could lead to infections if used improperly. Affected vials have specific batch numbers and expiration dates listed in the recall.
The vials may not be sterile, which can lead to infections if used for medical purposes. This lack of sterility assurance could cause serious health issues, especially for individuals with compromised immune systems or those using the supplements for medical treatments.
People who have purchased or are using the recalled Methionine/Inositol/Choline B12 vials from Tailor Made Compounding. Those with medical conditions requiring these supplements are at higher risk.
Check the batch numbers on the vial: 12092105A2, 01042219A2, 01202210A2, 01282207A1, 03032217A1, or 03032241A1. The vials are labeled as 10 mL or 30 mL and were sold at room temperature.
Look for batch numbers 12092105A2, 01042219A2, 01202210A2, 01282207A1, 03032217A1, or 03032241A1 on the vial.
Tailor Made Compounding is recalling specific batches of Methionine/Inositol/Choline B12 vials due to a lack of sterility assurance.
Check the batch numbers on the vial: 12092105A2, 01042219A2, 01202210A2, 01282207A1, 03032217A1, or 03032241A1.
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-1214-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1214-2022 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.
