Device recall
Z-0001-2012: Probe, Tactile, Left, ASM, Long, Part #962009S, Medtronic Navigation…
FDA device recall · Class II · Medtronic Navigation, Inc
Key facts
| Recall number (Z-number) | Z-0001-2012 |
|---|---|
| Recall event | 57858 |
| Product | Probe, Tactile, Left, ASM, Long, Part #962009S, Medtronic Navigation, Louisville, CO 80027. Trackable hand held instruments used in spine surgeries for preparation of the pedicle. These instruments are used in conjunction with the Medtronic Navigation StealthStation platform and various software… |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 3, 2011 |
| 510(k) numbers | K990214 |
| 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