FDA Device recall Z-0003-2023
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in…
- FDA Device
- Class II
- ongoing
- Published 2022-10-12
On 2022-10-12 the FDA classified a Class II recall of The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in… by In My Bathroom, citing excessive ultraviolet-C radiation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0003-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-01-27 |
| Published | 2022-10-12 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | In My Bathroom |
| Distribution | US |
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.
Reason
Excessive ultraviolet-C radiation
Identifiers
| code_info | Model Seago SG-153 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0003-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.