Recall Z-0457-2023— PHONESOAP
Class II · Ongoing
Class II FDA medical device recall by PHONESOAP, initiated 2022-08-30. 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 narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.. Reason: Excessive ultraviolet-C radiation.
- Recalling firm
- PHONESOAP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-08-30
- Firm location
- Provo, UT, United States
Product description
The product is a handheld ultraviolet-C germicidal wand and contains 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.