Device recall
Z-0623-2016: Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of…
FDA device recall · Class II · ArthroCare Corporation
Key facts
| Recall number (Z-number) | Z-0623-2016 |
|---|---|
| Recall event | 72789 |
| Product | Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures. |
| Product code | GEI |
| Recalling firm | ArthroCare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2016 |
| 510(k) numbers | K063172 |
| FEI number | 3010813691 |
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