Device recall
Z-1878-2025: Lazervida 10W diode laser cutter and engraver with Lazervida shield.
FDA device recall · Class II · Flux Technology Inc.
Key facts
| Recall number (Z-number) | Z-1878-2025 |
|---|---|
| Recall event | 96935 |
| Product | Lazervida 10W diode laser cutter and engraver with Lazervida shield. |
| Product code | RHK |
| Recalling firm | Flux Technology Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015156297 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database