Device recall
Z-1749-2015: ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw…
FDA device recall · Class II · Orthofix, Inc
Key facts
| Recall number (Z-number) | Z-1749-2015 |
|---|---|
| Recall event | 71297 |
| Product | ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw, Standard Implant Grade Titanium Alloy Rx Only Provided Non-Sterile Do Not Reuse |
| Product code | NKB |
| Recalling firm | Orthofix, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 30, 2015 |
| 510(k) numbers | K130932 |
| FEI number | 2183449 |
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