THOR Photomedicine recalls
3 official recalls and safety alerts involving THOR Photomedicine since 2023-12, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with THOR Photomedicine or the relevant agency.
- 2025-09-03
USTHOR Photomedicine Ltd recalls Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The…
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.
FDA · DeviceTHOR Photomedicine LtdWorldwide distribution: US (nationwide): AK, AZ, CA, CO, CT, FL, GA, HI, ID,…Official notice →- 2024-02-07
- US
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 Code S2190 - XL
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
FDA · DeviceTHOR Photomedicine LtdDomestic distribution to the states of Arizona California Colorado Connecticut…Official notice → - 2023-12-13
- US
Thor Photomedicine Ltd recalls NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
FDA · DeviceThor Photomedicine LtdWorldwide Distribution: US (Nationwide): Arizona, California, Colorado,…Official notice →