MAX LUX CORP recalls The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak em…
- Recall date
- October 26, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0246-2022
- FDA classification
- Class II
- Brand / firm
- MAX LUX CORP
- Sold / distributed
- US Nationwide Distribution
Why it was recalled
Excessive ultraviolet-C radiation
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
Get recall alerts
Free email alert whenever MAX LUX CORP has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: MAX LUX CORP