FDAAugust 1, 2022device
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 recorded by the U.S. Food & Drug Administration.
The hazard
Excessive ultraviolet-C radiation
What to do
FDA enforcement status: Ongoing
Brands named
merchsource
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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