Glutathione Preserved for Injection recalled over sterility concerns
- Recall date
- July 30, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- GenoGenix LLC recalls Glutathione Preserved for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton…
- Recall number
- D-0053-2026
- FDA classification
- Class II
- Brand / firm
- GenoGenix LLC
- Sold / distributed
- US Nationwide.
Why it was recalled
Lack of Assurance of Sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Glutathione Preserved for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Get recall alerts
Free email alert whenever GenoGenix LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: GenoGenix LLC