Z-0003-2023 Class II Ongoing

Recalled by IN MY BATHROOM LLC — Woodland Hills, CA

Recall Details

Product Type
Devices
Report Date
October 12, 2022
Initiation Date
January 27, 2022
Termination Date
N/A
Voluntary/Mandated
FDA Mandated
Product Quantity
485 units

Product Description

The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

Reason for Recall

Excessive ultraviolet-C radiation

Distribution Pattern

US Nationwide Distribution

Code Information

Model Seago SG-153