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Diowave Laser System, REF: Diowave 250W

Class II
Recalling firm
Technological Medical Advancements LLC
Reason for recall
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.
Distribution pattern
US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
State
FL
Status
Ongoing
Recall number
Z-2162-2026
Recall initiated
January 9, 2026
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