Device recall
Z-0896-2013: Firebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod…
FDA device recall · Class II · Orthofix, Inc
Key facts
| Recall number (Z-number) | Z-0896-2013 |
|---|---|
| Recall event | 64265 |
| Product | Firebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod Connector (52-6700). Product Usage: The connector assemblies allow for rod components to be connected side-to-side, or end-to-end and eliminate the need of rebuilding the entire system with a longer rod in order to… |
| Product code | KWP |
| Recalling firm | Orthofix, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2013 |
| 510(k) numbers | K080407 |
| FEI number | 2183449 |
At a glance
- 1–9 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