Z-0246-2022 Class II Ongoing

Recalled by MAX LUX CORP — Yangjiangyangjiang

Recall Details

Product Type
Devices
Report Date
December 8, 2021
Initiation Date
October 26, 2021
Termination Date
N/A
Voluntary/Mandated
FDA Mandated
Product Quantity
9900 units

Product Description

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.

Reason for Recall

Excessive ultraviolet-C radiation

Distribution Pattern

US Nationwide Distribution

Code Information

Safe-T Lite