FDAFDA · Food and drugs·Recall number Z-0246-2022
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
Published December 8, 2021 · Recall initiated: October 26, 2021
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Excessive ultraviolet-C radiation
What to do
FDA Mandated · Letter
Recall details
- Manufacturer
- MAX LUX CORP
- Distributor
- US Nationwide Distribution
- Lot
- Safe-T Lite
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- China
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