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Technological Medical Advancements LLC recalls Diowave Laser System, REF: Diowave 250W
Recalled May 20, 2026 · FDA recall Z-2162-2026 · Technological Medical Advancements
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. · FDA Class II
Units
16
Sold at
US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
Description
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.
Product
Diowave Laser System, REF: Diowave 250W
Manufacturer(s)
Technological Medical Advancements LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →