Device recall
Z-1466-2015: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage…
FDA device recall · Class II · Biomet Spine, LLC
Key facts
| Recall number (Z-number) | Z-1466-2015 |
|---|---|
| Recall event | 70832 |
| Product | Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cervical spine with an interspinous fixation device. |
| Product code | HXC |
| Recalling firm | Biomet Spine, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2015 |
| FEI number | 3012447612 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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