PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: September 24, 2025 Initiated: August 29, 2025 #Z-2571-2025

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.

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.

Details

Recalling Firm
BigTree Sales Inc.
Units Affected
N/A
Distribution
U.S.A
Location
Arcadia, CA

Frequently Asked Questions

What product was recalled?
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.. Recalled by BigTree Sales Inc.. Units affected: N/A.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 24, 2025. Severity: Moderate. Recall number: Z-2571-2025.