Device recall
Z-1480-2015: Captiva's lumbar intervertebral fusion system Reamers (color code rings on the…
FDA device recall · Class II · Captiva Spine, Inc
Key facts
| Recall number (Z-number) | Z-1480-2015 |
|---|---|
| Recall event | 70710 |
| Product | Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers). |
| Product code | LXH |
| Recalling firm | Captiva Spine, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 1, 2015 |
| FEI number | 3006082533 |
At a glance
- None 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