FDA Device recall Z-1878-2025
Lazervida 10W diode laser cutter and engraver with Lazervida shield
- FDA Device
- Class II
- ongoing
- Published 2025-06-11
On 2025-06-11 the FDA classified a Class II recall of Lazervida 10W diode laser cutter and engraver with Lazervida shield by Flux Technology, citing 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 a….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1878-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-19 |
| Published | 2025-06-11 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Flux Technology |
| Distribution | n/a |
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.
Identifiers
| code_info | None. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1878-2025%22
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