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FDAJuly 30, 2025drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Microbial Contamination of Sterile Products: elevated endotoxin levels

What to do

FDA enforcement status: Ongoing

Brands named

genogenix

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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