Device recall
Z-2870-2017: X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400…
FDA device recall · Class II · X-Laser Llc
Key facts
| Recall number (Z-number) | Z-2870-2017 |
|---|---|
| Recall event | 77843 |
| Product | X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500 High-power laser light show projector. |
| Product code | REA |
| Recalling firm | X-Laser Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 16, 2024 |
| FEI number | 3010087512 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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