Thor Photomedicine Ltd has recalled 77 NovoTHOR whole body red light therapy beds because a critical component called a ball stud can fail. This failure causes the gas strut that supports the heavy canopy to detach on one side, making the lid very difficult to lift and potentially allowing it to fall unexpectedly. The recall includes four specific models—Gen 2.0, Gen 2.0 XL, Gen 2.5 Regular, and Gen 2.5 XL—sold worldwide and across 22 U.S. states.
The failure of the ball stud components causes the gas-filled support strut to detach, which removes the mechanical assistance required to hold up the heavy canopy. This poses a physical injury risk if the canopy becomes difficult to maneuver or falls unexpectedly on a user.
Manufacturer-initiated corrective action.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.