Flux Technology Inc.: Device Recall
Recall #Z-1878-2025 · 02/19/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1878-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Flux Technology Inc.
- Status
- Ongoing
- Date Initiated
- 02/19/2025
- Location
- Taipei City, N/A, Taiwan
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 91
Reason for Recall
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.
Product Description
Lazervida 10W diode laser cutter and engraver with Lazervida shield.
Distribution Pattern
US
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.