Device recall
Z-2316-2018: MX-10 surveillance laser system Product Usage: The expected usage of the product…
FDA device recall · Class II · Wescam Inc
Key facts
| Recall number (Z-number) | Z-2316-2018 |
|---|---|
| Recall event | 80392 |
| Product | MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges. |
| Product code | REP |
| Recalling firm | Wescam Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2021 |
| FEI number | 3000173214 |
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