FDA Recall Open, Classified

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.

Recall: Z-2571-2025 · Initiated August 29, 2025

Recall

Recall Number
Z-2571-2025
Event Number
97621
Firm
BigTree Sales Inc.
FEI Number
3039602167
Product Code
RHP
Status
Open, Classified
Root Cause
Radiation Control for Health and Safety Act
Initiated
August 29, 2025
Posted
September 18, 2025
Address
11715 Clark St, Arcadia, CA, 91006-5806

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

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.

Action

BigTree Sales, Inc. notified FDA and their customers as required by 21 CFR 1003.10(b), that their electronic product, Portable UV-C Light Sanitizer Wand/Travel UV Sanitizing Wand, model: HH1103/HD-UV-01PL03 (SKU BT-GERMWAND-LRG-WHT), has been discovered to contain a defect related to its safety. Their customer letter was sent with the knowledge of the U.S. Food and Drug Administration (FDA).

Distribution

U.S.A