Class II
Medical Device Recall: Lazervida 10W diode laser cutter and engraver with Lazervida shield.
Flux Technology Inc. · February 19, 2025
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.
Distribution
US
Quantity Affected
91
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1878-2025
Status: ongoing
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