Device recall
Z-0839-2007: Silver Speed Hydrophilic Guidewire, for placement of vascular catheters. Model #…
FDA device recall · Class II · EV3 Neurovascular
Key facts
| Recall number (Z-number) | Z-0839-2007 |
|---|---|
| Recall event | 37821 |
| Product | Silver Speed Hydrophilic Guidewire, for placement of vascular catheters. Model # 103-0601-200. |
| Product code | MKI |
| Recalling firm | EV3 Neurovascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2012 |
| 510(k) numbers | K982543 |
| FEI number | 3004904811 |
At a glance
- 1–9 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