Device recall
Z-0265-2014: ATTAIN HYBRID Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain…
FDA device recall · Class I · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-0265-2014 |
|---|---|
| Recall event | 66567 |
| Product | ATTAIN HYBRID Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain Hybrid guide wire is intended to aid in the placement of Medtronic transvenous left ventricular leads in the coronary vasculature. |
| Product code | DQX |
| Recalling firm | Medtronic Vascular |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 15, 2014 |
| 510(k) numbers | K063210 |
| FEI number | 1220452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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