Thor Photomedicine Ltd: Medical Device Recall in 2023 - (Recall #: Z-0456-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.

Product Classification:

Class II

Date Initiated: September 13, 2022

Date Posted: December 13, 2023

Recall Number: Z-0456-2024

Event ID: 93344

Reason for Recall:

Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

Status: Ongoing

Product Quantity: 26

Code Information:

Serial numbers: 3025, 3026, 3027, 3030, 3031, 3034, 3035, 3036, 3037, 3038, 3039, 3040, 3042, 3043, 3044, 3045, 3047, 3050, 3051, 3053.

Distribution Pattern:

Worldwide Distribution: US (Nationwide): Arizona, California, Colorado, Connecticut, Florida, Hawaii, Idaho, Illinois, Iowa, Maryland, Michigan, Minnesota, Missouri, Nevada, New Hampshire, North Carolina, Ohio, Oregon, Texas, Utah, Virginia, West Virginia. OUS (foreign) to countries of: Australia, Canada, Netherlands, New Zealand, Singapore, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated