Device recall
Z-2100-2019: Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage…
FDA device recall · Class II · ASTRA, LLC
Key facts
| Recall number (Z-number) | Z-2100-2019 |
|---|---|
| Recall event | 83302 |
| Product | Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access |
| Product code | RFC |
| Recalling firm | ASTRA, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015494597 |
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