Reported Oct 15, 2025 · Ongoing
NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials,…
GenoGenix LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GenoGenix LLC · 2840 Nw 2nd Ave Ste 204 · Boca Raton, FL · 33431-6692
Is this the product you have?
- NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
- Lot codes and dates
- Lot#: GG121624-023, within expiry
This recall covers 57 products
The agency filed one notice per product. You are reading one of them; the other 56 are below.
44 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Microbial Contamination of Sterile Products: elevated endotoxin levels
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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