Recall archive / FDA device enforcement
Lazervida 10W diode laser cutter and engraver with Lazervida shield. — FDA record Z-1878-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 19, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Lazervida 10W diode laser cutter and engraver with Lazervida shield.
- 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.
- Classification
- Class II
- Recalling firm
- Flux Technology Inc.
- Quantity
- 91
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1878-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | None. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Jun 11, 2025
- Recall initiation date
- Feb 19, 2025
- Center classification date
- Jun 3, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.