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THOR Photomedicine Recalls

9 recalls on record · December 13, 2023 to September 3, 2025 · Medical Devices

Recalls by year

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25

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

September 3, 2025Medical DevicesFDA
THOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product De
Hazard: The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
September 3, 2025Medical DevicesFDA
THOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product De
Hazard: The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
September 3, 2025Medical DevicesFDA
THOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: Th
Hazard: The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
September 3, 2025Medical DevicesFDA
THOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The N
Hazard: The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
February 7, 2024Medical DevicesFDA
THOR Photomedicine Ltd recalls NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Co
Hazard: One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy
December 13, 2023Medical DevicesFDA
Thor Photomedicine Ltd recalls NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.
Hazard: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
December 13, 2023Medical DevicesFDA
Thor Photomedicine Ltd recalls NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Hazard: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
December 13, 2023Medical DevicesFDA
Thor Photomedicine Ltd recalls G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
Hazard: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
December 13, 2023Medical DevicesFDA
Thor Photomedicine Ltd recalls NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
Hazard: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
THOR Photomedicine Recalls | RecallWatchUSA