Z-1878-2025 Class II Ongoing
FDA device recall Z-1878-2025 was initiated by Flux Technology Inc. on Feb 19, 2025 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 91.
Recall details
- Product Type
- Devices
- Report Date
- Jun 11, 2025
- Initiation Date
- Feb 19, 2025
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 91
Product description
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 pattern
US
Code information
None.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1878-2025
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026