Thor Photomedicine Ltd: Medical Device Recall in 2023 - (Recall #: Z-0455-2024)

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 Regular whole body red light therapy bed, model S2183

Product Classification:

Class II

Date Initiated: September 13, 2022

Date Posted: December 13, 2023

Recall Number: Z-0455-2024

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: 2002, 2050, 2051, 2052, 2053, 2054, 2055, 2056, 2057, 2059, 2060, 2061, 2062, 2064, 2065, 2066, 2075, 2076, 2077, 2078, 2081, 2084, 2085, 2086, 2088, 2089, 2090, 2094, 2097.

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