PHONESOAP recalls The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emissio…

Recall date

August 30, 2022

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0457-2023

FDA classification

Class II

Brand / firm

PHONESOAP

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 narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.