Device recall
Z-0616-2012: SideWinder Hip Wand Product Number AC2340-01 is an ablation wand Intended for…
FDA device recall · Class II · Innovatech Medical Resources L.P.
Key facts
| Recall number (Z-number) | Z-0616-2012 |
|---|---|
| Recall event | 60049 |
| Product | SideWinder Hip Wand Product Number AC2340-01 is an ablation wand Intended for resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic and orthopedic procedures |
| Recalling firm | Innovatech Medical Resources L.P. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2012 |
| 510(k) numbers | K082980 |
| FEI number | 3009124511 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
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