Recall Z-0003-2023— IN MY BATHROOM LLC
Class II · Ongoing
Class II FDA medical device recall by IN MY BATHROOM LLC, initiated 2022-01-27. FDA's recall record names no specific 510(k) clearance for this event. 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.
- Recalling firm
- IN MY BATHROOM LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-01-27
- Firm location
- Woodland Hills, CA, United States
Product description
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 for recall
Excessive ultraviolet-C radiation
Data sourced from openFDA. This site is unofficial and independent of the FDA.