FDA recall Z-1878-2025

Flux Technology Inc. · Class II · device

Product

Lazervida 10W diode laser cutter and engraver with Lazervida shield.

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

Key facts

Status
Ongoing
Initiation date
2025-02-19
Report date
2025-06-11
Voluntary/Mandated
FDA Mandated
Location
Taipei City, N/A, Taiwan

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1878-2025