Diowave Laser System, REF: Diowave 250W
Recall
- Recall Number
- Z-2162-2026
- Event Number
- 98507
- Firm
- Technological Medical Advancements LLC
- FEI Number
- 3009346095
- Product Code
- ILY
- Status
- Open, Classified
- Root Cause
- Under Investigation by firm
- Initiated
- January 9, 2026
- Posted
- May 11, 2026
- Address
- 1601 Belvedere Rd, Ste E-180, West Palm Beach, FL, 33406-1541
Description
Diowave Laser System, REF: Diowave 250W
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.
Starting on 1/9/2026, customer notifications were sent informing customers to install software update V1.81. On 3/11/2026, correction notices were sent to customers informing them to take the following actions: 1) Install Software Update V1.81. Follow the WiFi upgrade instructions to complete the update. The update is free of charge and requires no hardware modifications. 2) Confirm Completion. Once the update is installed, please complete and return the enclosed Correction Response Form by email to [email protected]. Alternatively, mail the completed form to TMA at the address above. 3) Forward This Notice. This notice must be passed on to all persons within your organization who need to be aware of this correction, and to any organization where the affected device has been transferred or is currently in use. 4) Contact Support If Needed. Firm's technical support team is available Monday through Friday, 9:00 AM 5:00 PM ET, at (561) 722-1153 or [email protected]
US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
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