PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: December 28, 2022 Initiated: August 30, 2022 #Z-0457-2023

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

Details

Recalling Firm
PHONESOAP
Units Affected
6,700 systems
Distribution
US Nationwide Distribution
Location
Provo, UT

Frequently Asked Questions

What product was recalled?
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.. Recalled by PHONESOAP. Units affected: 6,700 systems.
Why was this product recalled?
Excessive ultraviolet-C radiation
Which agency issued this recall?
This recall was issued by the FDA Devices on December 28, 2022. Severity: Moderate. Recall number: Z-0457-2023.