FDA Medical Device Recalls (openFDA)
IN MY BATHROOM LLC: 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.
- Recall number
- Z-0003-2023
- 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.
- Status
- Open, Classified
- Initiated
- 2022-01-27
- Posted
- 2022-10-05
- Terminated
- not on file
- Reason
- Excessive ultraviolet-C radiation
- 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
- 485 units
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- Model Seago SG-153
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- RHP
- Firm FEI
- 3016850352
- Firm city
- Woodland Hills
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28