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IN MY BATHROOM LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emi
Recalled October 12, 2022 · FDA recall Z-0003-2023 · IN MY BATHROOM
Hazard
Excessive ultraviolet-C radiation · FDA Class II
Units
485 units
Sold at
US Nationwide Distribution
Description
Excessive ultraviolet-C radiation
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.
Manufacturer(s)
IN MY BATHROOM LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →