FDA Recall
Open, Classified
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.
Recall: Z-0246-2022
·
Initiated October 26, 2021
Recall
- Recall Number
- Z-0246-2022
- Event Number
- 89050
- Firm
- MAX LUX CORP 03e 01 01 Yangxi Indust Ry Zone Yangjiangyangjiang China
- FEI Number
- 3017032819
- Product Code
- RHP
- Status
- Open, Classified
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- October 26, 2021
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
Excessive ultraviolet-C radiation
Distribution
US Nationwide Distribution
Quantity
9900 units