fda_recall · device_recall · high

Technological Medical Advancements LLC — Class II recall: Diowave Laser System, REF: Diowave 250W

Event date
2026-05-20 00:00:00Z
Observed
2026-07-09 22:52:31Z
Source ID
Z-2162-2026
Payload hash
20ba2077dcac93ffee872379

Summary

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 b… Status: Ongoing.

Informational only. Not legal, financial, or medical advice.