Device recall
Z-1042-2011: Vertex Max Drill Tube, Catalog Number 9733140, a component of the Navigated…
FDA device recall · Class II · Medtronic Navigation, Inc
Key facts
| Recall number (Z-number) | Z-1042-2011 |
|---|---|
| Recall event | 57549 |
| Product | Vertex Max Drill Tube, Catalog Number 9733140, a component of the Navigated Vertex Max Drill Guide Kit, Catalog Number 9733370. Medtronic, Inc., Louisville, CO. Used in conjunction with the StealthStation navigation systems to assist in screw placement during spine surgery. |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 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