IN MY BATHROOM LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak em…
- Recall date
- January 27, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0003-2023
- FDA classification
- Class II
- Brand / firm
- IN MY BATHROOM LLC
- Sold / distributed
- US Nationwide Distribution
Why it was recalled
Excessive ultraviolet-C radiation
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
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