THOR Photomedicine Ltd has recalled approximately 138 NovoTHOR, NovoTHOR XL, and NovoTHOR Gen 3.0 Reg PRX light therapy pods because a welded nut inside the device can fail and shear off. If this nut breaks, the gas strut that supports the pod's heavy canopy can detach on one side, making the canopy extremely difficult to lift or potentially unstable. The recall includes units distributed worldwide, with 108 of the affected pods located in the United States.
A failed welded nut causes the gas strut to detach from the canopy, which may lead to the heavy canopy falling or becoming difficult to control during use. This poses a risk of impact injuries to users or staff and could make it difficult for an occupant to exit the device safely.
Recall Z-2416-2025; Quantity 80 units.
Recall Z-2417-2025; Quantity 55 units.
Recall Z-2418-2025; Quantity 1 unit.
Recall Z-2419-2025; Quantity 2 units.
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.