Device recall
Z-0870-2020: EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very…
FDA device recall · Class II · Energetiq Technology Inc
Key facts
| Recall number (Z-number) | Z-0870-2020 |
|---|---|
| Recall event | 84378 |
| Product | EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the Deep UV through the visible wavelengths. |
| Product code | REK |
| Recalling firm | Energetiq Technology Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3005152898 |
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