FDAJanuary 9, 2026device

Diowave Laser System, REF: Diowave 250W

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

technological medical advancementstechnologicaltechnological medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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