Z-0003-2023Class II

The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with...

Name: Z-0003-2023 The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with...
Creator: In My Bathroom Llc
Published: 2022-01-27
License: https://open.fda.gov/license/

In My Bathroom LLC / initiated 2022-01-27 / Open, Classified

FDA source

IN MY BATHROOM LLC began a recall of 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 on 2022-01-27. FDA classified it as Class II and gives the reason as "Excessive ultraviolet-C radiation". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-0003-2023
Classification: Class II
Status: Open, Classified
Initiated: 2022-01-27
Posted: 2022-10-05
Recalling firm: In My Bathroom LLC
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.
Product code: RHP Uv Lamp, Germicidal
Reason for recall: Excessive ultraviolet-C radiation
FDA root cause: Radiation Control for Health and Safety Act
Action: The firm issued and Urgent Electronic Device Recall letter dated September 9, 2022. Please complete and return the Electronic Device Recall Return Response form below as soon as possible to acknowledge receipt of this letter and initiate the process of sending back your UVILIZER Flip (Model Seago SG-153).
Quantity in commerce: 485 units
Distribution: US Nationwide Distribution
Product codes and lots: Model Seago SG-153

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0003-2023
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0003-2023	Class II	Ongoing	FDA Mandated	2022-10-12	2022-10-05

Product code RHP

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)