The Recall Desk
HighFDA (Devices)·Z-0003-2023·Announced 2022-10-12

Handheld UV-C Germicidal Wand Recalled for Excessive Radiation Exposure

IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is an FDA Class II medical device recall for a risk-of-harm product where no injuries or illnesses have been reported in the source. Excessive UV-C radiation exposure without documented harm meets the High severity criterion.

Plain-English summary

IN MY BATHROOM LLC is recalling the Seago SG-153 handheld ultraviolet-C germicidal wand. The recall affects 485 units that were distributed nationwide in the United States. The device contains two narrow-diameter tubular lamps with a peak emission wavelength of 254 nanometers.

The product is being recalled due to excessive ultraviolet-C radiation. Consumers who have this product should stop using it and contact IN MY BATHROOM LLC for instructions on how to return or dispose of the device.

The recalled product

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.
Manufacturer
IN MY BATHROOM LLC
Category
Medical Device — UV-C Germicidal Device
Hazard
Affected units
485

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Model Seago SG-153

Distribution

Distributed nationwide across the United States.

Related recalls

Same hazard · uv c radiation

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