GenoGenix recalls NAD+ injections with elevated endotoxin levels. This microbial contamination may cause serious health risks. Affected products include 100 mg/mL and 200 mg/mL 10mL amber vials.
Microbial Contamination of Sterile Products: elevated endotoxin levels
GenoGenix is recalling NAD+ injections that may have elevated endotoxin levels due to microbial contamination. This could pose serious health risks to patients receiving the injections.
Elevated endotoxin levels in sterile products can cause serious infections or adverse reactions when injected into the body. Microbial contamination in injectable medications is a known risk for patients receiving treatments.
Patients using the recalled NAD+ injections for medical purposes are affected. Healthcare providers administering these injections to patients are at higher risk.
Check for GenoGenix NAD+ injections labeled 100 mg/mL or 200 mg/mL in 10 mL multi-dose amber vials. The products were sold with lot number GG121624-023 and within their expiration date.
Identify if your NAD+ injection is labeled 100 mg/mL or 200 mg/mL in 10 mL multi-dose amber vials with lot number GG121624-023.
Yes, patients using the recalled NAD+ injections may be at risk of serious health issues due to microbial contamination.
Check for GenoGenix NAD+ injections labeled 100 mg/mL or 200 mg/mL in 10 mL multi-dose amber vials with lot number GG121624-023.
The recall record does not specify a remedy, so contact GenoGenix directly 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-0094-2026 — GenoGenix GenoGenix Hello, I own a GenoGenix that is covered by recall D-0094-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.