Stop using now Medical device recall · FDA · Published January 27, 2022

IN MY BATH: Handheld UV-C Germicidal Wand Recall - Excessive UV-C Radiation Hazard

IN MY BATHROOM LLC recalls handheld UV-C germicidal wands (Model Seago SG-153) due to excessive UV-C radiation risk. Consumers should stop using the product immediately.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0003-2023Medical device IN MY BATHROOM LLC ›

Stop using this now

Excessive ultraviolet-C radiation

Take action

Contact the company

Recalling firmIN MY BATHROOM LLC22617 Mariano St · Woodland Hills, CA 91367-6127

✎ GovInfoNow plain-language explainer

IN MY BATHROOM LLC is recalling their handheld UV-C germicidal wands (Model Seago SG-153) because they emit excessive ultraviolet-C radiation that could cause skin damage. This recall is important because UV-C radiation can harm skin and eyes when exposed to directly. Read more at govinfonow.com/recall/61219-in-my-bath-handheld-uv-c-germicidal-wand-recall-excessive.

Source Summary by GovInfoNow · govinfonow.com/recall/61219-in-my-bath-handheld-uv-c-germicidal-wand-recall-excessive · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0003-2023

Cite this page

“IN MY BATH: Handheld UV-C Germicidal Wand Recall - Excessive UV-C Radiation Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61219-in-my-bath-handheld-uv-c-germicidal-wand-recall-excessive. Based on FDA recall #Z-0003-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0003-2023%22&limit=1).

IN MY BATHROOM LLC recalled handheld ultraviolet-C germicidal wands due to excessive ultraviolet-C radiation hazards, according to the FDA. The Food and Drug Administration announced the Class II recall on Jan. 27, 2022.

How to tell if you have it

Brand: IN MY BATHROOM LLC
Model: Seago SG-153
Quantity: 485 units

The hazard

The handheld ultraviolet-C germicidal wand contains two narrow-diameter tubular lamps with a peak emission wavelength in the 254 nm range, posing a risk of excessive ultraviolet-C radiation exposure.

Context

GovInfoNow's records show other recent recalls of similar products include Uvlizer Germicidal Wand Recalls: UVC Radiation Exposure Risk (2026-03-06) and Uvlizer UV Germicidal Wand Recalls: Risk of Excessive UVC Exposure (2026-03-06). Lutronic DermaV Laser System Recall: Risk of Patient Burn During Treatment was also reported on 2026-08-06.

How to tell if you have this one

Check for the Seago SG-153 model number on the wand. The product was sold as a handheld UV-C germicidal wand with two narrow-diameter tubular lamps.

Brand
IN MY BATHROOM LLC
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using It Now
Immediately stop using the wand and do not expose yourself to the UV-C radiation.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 8 months after the firm started it.

Jan 27, 2022Firm started the recall
Oct 5, 2022FDA classified it Class II
Oct 12, 2022Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/61219-in-my-bath-handheld-uv-c-germicidal-wand-recall-excessive">IN MY BATH: Handheld UV-C Germicidal Wand Recall - Excessive UV-C Radiation Hazard (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0003-2023 (January 27, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0003-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.