Device recall
Z-2095-2019: Maxim Laser Projection Series
FDA device recall · Class II · Gk Photonics Inc
Key facts
| Recall number (Z-number) | Z-2095-2019 |
|---|---|
| Recall event | 83438 |
| Product | Maxim Laser Projection Series |
| Product code | REA |
| Recalling firm | Gk Photonics Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3006314809 |
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