MAX LUX CORP: Medical Device Recall in 2021 - (Recall #: Z-0246-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

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 with an intended use of disinfecting surfaces.

Product Classification:

Class II

Date Initiated: October 26, 2021

Date Posted: December 8, 2021

Recall Number: Z-0246-2022

Event ID: 89050

Reason for Recall:

Excessive ultraviolet-C radiation

Status: Ongoing

Product Quantity: 9900 units

Code Information:

Safe-T Lite

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated