Device recall
Z-0330-06: Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482
FDA device recall · Class III · Medtronic Sofamor Danek Instrument Manufacturing
Key facts
| Recall number (Z-number) | Z-0330-06 |
|---|---|
| Recall event | 34196 |
| Product | Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482 |
| Product code | HXX |
| Recalling firm | Medtronic Sofamor Danek Instrument Manufacturing |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 9, 2006 |
| FEI number | 3004564008 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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