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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:196079

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.

Official recall number

Z-0003-2023

Evidence summary

Product code
RHP
Recall status
Open, Classified
Event initiated
January 27, 2022
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0003-2023