West Palm Beach, FL, United States
Technological Medical Advancements LLC recalls
1 recall recorded since 2018, most recently on 9 January 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 9 January 2026
- Reason
- 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.
- Distribution
- US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2162-2026
- Diowave Laser System, REF: Diowave 250W
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.