Technological Medical Advancements LLC recalls Diowave Laser System, REF: Diowave 250W

Recall date

January 9, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2162-2026

FDA classification

Class II

Brand / firm

Technological Medical Advancements LLC

Sold / distributed

US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Diowave Laser System, REF: Diowave 250W