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FDA (Device enforcement)Recalled 2026-01-09class ii

Technological Medical Advancements LLC: 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.

Details from the source

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. Quantity: 16 Lot/code info: UDI-DI: G180DIOWAVESTEALTHMAX0. All software versions prior to, but not including V1.81

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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