Device recall
Z-2309-2008: ArthroCare ArthroWand Covator with Integrated Cable Wand, Catalog number…
FDA device recall · Class II · ArthroCare Corporation
Key facts
| Recall number (Z-number) | Z-2309-2008 |
|---|---|
| Recall event | 48731 |
| Product | ArthroCare ArthroWand Covator with Integrated Cable Wand, Catalog number AC4340-01. The product is a medical device for human use in electrosurgical cutting and coagulation accessories. Product is indicated for resection, ablation and coagulation of soft tissue and hemostasis of blood vessels in… |
| Product code | GEI |
| Recalling firm | ArthroCare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 14, 2011 |
| 510(k) numbers | K033584 |
| 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