May 20, 2026Medical DevicesFDA
Technological Medical Advancements LLC recalls Diowave Laser System, REF: Diowave 250W
Hazard: Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.