Tailor Made Compounding recalls NAD+ 200mg/mL vials with specific batch numbers 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 NAD+ 200mg/mL vials because they may not be sterile. Using these vials could lead to infections or other health risks if the product is contaminated.
The vials may not be sterile, meaning they could contain harmful bacteria or other contaminants. This poses a risk of infection or other health issues if the product is used without proper sterility.
People who purchased or use Tailor Made Compounding's NAD+ 200mg/mL vials with the listed batch numbers. Those with medical conditions requiring this supplement may be at higher risk.
Check the batch numbers on the vial: 10072110A2, 10142102A1, 01112205A1, 11112123A1, 11222114A1, 11172107A1, 11182120A2, 01102207A1, 01122211A1, 12162119A1, 12162121A1, 02022223A2, 03012204A1, 03082249B, 03092226B, 03092236B. These vials were sold with specific expiration dates.
Look for the batch numbers listed in the recall notice to determine if your vial is affected.
The recalled batch numbers are 10072110A2, 10142102A1, 01112205A1, 11112123A1, 11222114A1, 11172107A1, 11182120A2, 01102207A1, 01122211A1, 12162119A1, 12162121A1, 02022223A2, 03012204A1, 03082249B, 03092226B, 03092236B.
Check the batch number on your vial against the list provided in the recall notice.
The recall notice 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-1219-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1219-2022 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.
