Tailor Made Compounding recalls NAD+ 200mg/ml 10ml vials due to lack of sterility assurance. Affected lots: 07192307A2, BUD: 11/18/2023. No remedy specified.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling NAD+ 200mg/ml 10ml vials because they may not be sterile. This could lead to infections if used improperly. The recall affects specific lots with a batch number and expiration date.
The vials lack assurance of sterility, meaning they could be contaminated with bacteria or other pathogens. If used for injections, this could cause serious infections or other health issues.
People who purchased or use the recalled NAD+ 200mg/ml 10ml vials from Tailor Made Compounding. Those with medical conditions requiring sterile injections are at higher risk.
Check for the lot number 07192307A2 on the vial label. The vials were sold with a use-by date of November 18, 2023.
Look for the lot number 07192307A2 and use-by date of November 18, 2023 on the vial.
The official recall notice does not specify a remedy.
The lot number is 07192307A2.
The vials were sold with a use-by date of November 18, 2023.
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-1106-2023 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1106-2023 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.
