Official recall record
Diowave Laser System, REF: Diowave 250W
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-01-09
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- Technological Medical Advancements LLC
What the authority reported
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
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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