GenoGenix recalls NAD+ 50 mg/mL and 100 mg/mL 10mL multi-dose vials due to lack of sterility assurance. Affected products may pose infection risks if used.
Lack of Assurance of Sterility
GenoGenix is recalling NAD+ vitamin supplements in 50 mg/mL and 100 mg/mL 10mL multi-dose vials because they lack sterility assurance. This could lead to infections if the product is used.
The vials lack proper sterility assurance, meaning they could become contaminated with bacteria or other pathogens. If the product is used without proper sterilization, it could cause infections.
People who purchased GenoGenix NAD+ supplements in 50 mg/mL or 100 mg/mL 10mL multi-dose vials. Those using the product for medical purposes are at higher risk.
Check for GenoGenix NAD+ vials labeled 50 mg/mL or 100 mg/mL with 10mL capacity. Products were sold by GenoGenix LLC in Boca Raton, Florida, and may have been manufactured for CELIA Health.
Identify if your NAD+ vials are labeled 50 mg/mL or 100 mg/mL with 10mL capacity.
No, this recall specifically affects GenoGenix NAD+ 50 mg/mL and 100 mg/mL 10mL multi-dose vials.
Check for GenoGenix NAD+ vials labeled 50 mg/mL or 100 mg/mL with 10mL capacity. Products were sold by GenoGenix LLC in Boca Raton, Florida.
The recall record does not specify a remedy, so contact GenoGenix LLC for guidance.
We’ve drafted a message you can send GenoGenix to request your refund or repair — edit it as you like.
Subject: Recall D-0065-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0065-2026 from GenoGenix. 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.