Device recall
Z-0718-06: AxiEM EM Knee Kit, and associated workstation.
FDA device recall · Class III · Medtronic Navigation, Inc
Key facts
| Recall number (Z-number) | Z-0718-06 |
|---|---|
| Recall event | 34604 |
| Product | AxiEM EM Knee Kit, and associated workstation. |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 6, 2006 |
| 510(k) numbers | K001284, K043088 |
| FEI number | 1000517638 |
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