FDAMarch 6, 2026device
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
What to do
FDA enforcement status: Ongoing
Brands named
uvlizer c o raisuvlizer
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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