Device recall
Z-3073-2011: Habib, 4x Kit, Bipolar Resection Device RITA (Radiofrequency Ablation Devices)…
FDA device recall · Class II · Angiodynamics, INC
Key facts
| Recall number (Z-number) | Z-3073-2011 |
|---|---|
| Recall event | 59680 |
| Product | Habib, 4x Kit, Bipolar Resection Device RITA (Radiofrequency Ablation Devices). AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816. Intended to be used to assist in coagulation of tissue during intraoperative surgical procedures. |
| Product code | GEI |
| Recalling firm | Angiodynamics, INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 12, 2012 |
| 510(k) numbers | K051420 |
| FEI number | 3017892510 |
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