FDA recall Z-0457-2023

Product

The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

Reason for recall

Excessive ultraviolet-C radiation

Distribution

US Nationwide Distribution

Key facts

Status

Ongoing

Initiation date

2022-08-30

Report date

2022-12-28

Voluntary/Mandated

FDA Mandated

Location

Provo, UT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0457-2023