Medical Device Recall: Diowave Laser System, REF: Diowave 250W
Technological Medical Advancements LLC · January 9, 2026
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
US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
States Affected
NATIONWIDE
Quantity Affected
16
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2162-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.