IN MY BATHROOM LLC: Medical Device Recall in 2022 - (Recall #: Z-0003-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: January 27, 2022

Date Posted: October 12, 2022

Recall Number: Z-0003-2023

Event ID: 90860

Reason for Recall:

Excessive ultraviolet-C radiation

Status: Ongoing

Product Quantity: 485 units

Code Information:

Model Seago SG-153

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated