FDAAugust 29, 2025device

The product is a handheld ultraviolet-C germicidal wand and contains a 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

The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.

What to do

FDA enforcement status: Ongoing

Brands named

bigtree salesbigtree

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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