Device recall
Z-0172-2010: MX Series Products, Model numbers MX 20, MX 20 High Definition (HD), MX 15, MX…
FDA device recall · Class II · Wescam Inc
Key facts
| Recall number (Z-number) | Z-0172-2010 |
|---|---|
| Recall event | 53809 |
| Product | MX Series Products, Model numbers MX 20, MX 20 High Definition (HD), MX 15, MX 15i (integrated) and MX 15 HDi. Long range surveillance, target designation. |
| Product code | RET |
| Recalling firm | Wescam Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2013 |
| 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