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Thor Photomedicine Ltd recalls NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Recalled December 13, 2023 · FDA recall Z-0455-2024 · Thor Photomedicine
Hazard
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. · FDA Class II
Units
26
Sold at
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.
Description
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
Product
NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Manufacturer(s)
Thor Photomedicine Ltd
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →