BigTree Sales Inc.: Device Recall
Recall #Z-2571-2025 · 08/29/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2571-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- BigTree Sales Inc.
- Status
- Ongoing
- Date Initiated
- 08/29/2025
- Location
- Arcadia, CA, United States
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- N/A
Reason for Recall
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.
Product Description
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.
Distribution Pattern
U.S.A
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.