Device recall
Z-0579-2015: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger Switches…
FDA device recall · Class II · ArthroCare Medical Corporation
Key facts
| Recall number (Z-number) | Z-0579-2015 |
|---|---|
| Recall event | 69667 |
| Product | Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger Switches and Model Number ASHA5050-01: Ambient KVac Wand with Integrated Finger Switches. The Wands are indicated for the resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic and… |
| Product code | GEI |
| Recalling firm | ArthroCare Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 9, 2015 |
| 510(k) numbers | K083306 |
| 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