Device recall
Z-1489-04: Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and…
FDA device recall · Class II · Medtronic Inc
Key facts
| Recall number (Z-number) | Z-1489-04 |
|---|---|
| Recall event | 30016 |
| Product | Medtronic DLP VAD Venous Cannula for Ventricular Assist, Models 95036 and CB95036. |
| Product code | DWF |
| Recalling firm | Medtronic Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 3, 2005 |
| 510(k) numbers | K845045 |
| FEI number | 3001504994 |
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