Recall Z-0246-2022— MAX LUX CORP
Class II · Ongoing
Class II FDA medical device recall by MAX LUX CORP, initiated 2021-10-26. FDA's recall record names no specific 510(k) clearance for this event. Product: 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.
- Recalling firm
- MAX LUX CORP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-10-26
- Firm location
- Yangjiangyangjiang, China
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.