Reported May 20, 2026 · Ongoing
Diowave Laser System, REF: Diowave 250W
Technological Medical Advancements LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Technological Medical Advancements LLC · 1601 Belvedere Rd Ste E-180 · West Palm Beach, FL · 33406-1541
Is this the product you have?
- Diowave Laser System
- REFDiowave 250W
- Lot codes and dates
- UDI-DIG180DIOWAVESTEALTHMAX0. All software versions prior to, but not including V1.81
- Amount recalled
- 16
Where it was sold
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.
This product could cause temporary or reversible health problems — stop using it.
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