Taipei City, N/A, Taiwan
Flux Technology Inc. recalls
1 recall recorded since 2018, most recently on 19 February 2025. 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
- 19 February 2025
- Reason
- Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector, key switch, specific labels and manual instructions required under current regulations.
- Distribution
- US
- Initiated
- FDA Mandated
- Recall number
- Z-1878-2025
- Lazervida 10W diode laser cutter and engraver with Lazervida shield.
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.