Yangjiangyangjiang, China
MAX LUX CORP recalls
1 recall recorded since 2018, most recently on 26 October 2021. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 26 October 2021
- Reason
- Excessive ultraviolet-C radiation
- Distribution
- US Nationwide Distribution
- Initiated
- FDA Mandated
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.