Device recall
Z-0145-2011: Vertex Max Drill Guide, Catalog Number 9732355, to be used with a Medtronic…
FDA device recall · Class II · Medtronic Navigation, Inc
Key facts
| Recall number (Z-number) | Z-0145-2011 |
|---|---|
| Recall event | 56893 |
| Product | Vertex Max Drill Guide, Catalog Number 9732355, to be used with a Medtronic Computer-Assisted Surgery System to help assist with screw placement during spine procedures. To be used with a Medtronic Computer-Assisted Surgery System to help assist with screw placement during spine procedures. |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2011 |
| 510(k) numbers | K050438 |
| 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