PlainRecalls
FDA Devices Moderate Class II Ongoing

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

Reported: December 13, 2023 Initiated: September 13, 2022 #Z-0453-2024

Product Description

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

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.

Details

Recalling Firm
Thor Photomedicine Ltd
Units Affected
19
Distribution
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.
Location
Chesham

Frequently Asked Questions

What product was recalled?
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176. Recalled by Thor Photomedicine Ltd. Units affected: 19.
Why was this product recalled?
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 13, 2023. Severity: Moderate. Recall number: Z-0453-2024.