Every recall we track for THOR Photomedicine Ltd — 9 in all — plus the complaints and injury reports the public filed about them.
THOR recalls NovoTHOR model S2188 devices due to potential welded nut failure causing canopy detachment. Affected units have specific serial numbers; stop using immediately to prevent injury.
THOR recalls one NovoTHOR Gen 3.0 Reg PRX device (model S2189) due to potential welded nut failure causing canopy detachment. Affected units may have difficulty lifting the canopy. No remedy specified.
THOR recalls NovoTHOR XL devices with model S2190 due to potential welded nut failure causing canopy detachment. Affected units may have difficulty lifting the canopy if the gas strut becomes disconnected.
THOR recalls NovoTHOR Gen 3.0 Reg PRX model S2186 due to potential welded nut failure causing canopy detachment. Affected units have serial numbers 4005 or 4062. Stop using immediately to prevent injury.
THOR Photomedicine recalls NovoTHOR Whole Body Light Pod Gen 3.0 models with potential canopy failure risk. Affected units may cause injury if a ball stud fails during canopy operation.
NovoTHOR Gen 2.5 XL whole body red light therapy bed model S2184 with serial numbers 3025-3053 recalled due to risk of canopy detachment. Consumers should stop using affected units immediately.
THOR Photomedicine Ltd recalls G041 POD whole body red light therapy beds with serial numbers 3001-3009. Failure of ball stud components may cause canopy detachment during use.
NovoTHOR Gen 2.0 whole body red light therapy bed model S1176 with specific serial numbers recalled due to risk of canopy detachment during use. Affected units may have difficulty lifting the canopy safely.
Thor Photomedicine recalls NovoTHOR Gen 2.5 whole body red light therapy beds (model S2183) due to risk of canopy detachment from gas strut failure. Affected units have specific serial numbers listed in the recall.
