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Recall Observatory FDA recall evidence

Device product

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.

Z-0003-2023

January 27, 2022

Class II

Product summary

Firm
IN MY BATHROOM LLC
Event
Event 90860
Status
Ongoing
Classification
Class II
Quantity
485 units
Official record key
device-enforcement:Z-0003-2023

Official wording

Reason: Excessive ultraviolet-C radiation

Code information: Model Seago SG-153

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Excessive ultraviolet-C radiation