PHONESOAP: Medical Device Recall in 2022 - (Recall #: Z-0457-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: August 30, 2022

Date Posted: December 28, 2022

Recall Number: Z-0457-2023

Event ID: 91221

Reason for Recall:

Excessive ultraviolet-C radiation

Status: Ongoing

Product Quantity: 6,700 systems

Code Information:

SurfaceSoap UV Disinfecting Wand

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated