Device recall
Z-0207-05: Medtronic CapSureFix Novus Lead Model 5076.
FDA device recall · Class III · Medtronic Inc. Cardiac Rhythm Managment
Key facts
| Recall number (Z-number) | Z-0207-05 |
|---|---|
| Recall event | 30369 |
| Product | Medtronic CapSureFix Novus Lead Model 5076. |
| Product code | DTA |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Managment |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 24, 2005 |
| PMA numbers | P930039, P930039S009 |
| FEI number | 2182208 |
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