The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emi... — FDA record Z-2571-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 29, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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.
Reason
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.
Classification
Class II
Recalling firm
BigTree Sales Inc.
Quantity
N/A
Agency-reported status
Ongoing
Source record identifier
Z-2571-2025

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What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilitySKU BT-GERMWAND-LRG-WHT and Testing: September 8-10, 2020

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

U.S.A

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Report date
Sep 24, 2025
Recall initiation date
Aug 29, 2025
Center classification date
Sep 18, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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