Device recall
Z-0663-2007: RF Denervation Probe, 10 cm, temperature sensing electrodes designed for use in…
FDA device recall · Class I · Smith & Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-0663-2007 |
|---|---|
| Recall event | 37232 |
| Product | RF Denervation Probe, 10 cm, temperature sensing electrodes designed for use in radiofrequency lesion procedures for the treatment of pain. Product Number: 7210271 |
| Product code | GXI |
| Recalling firm | Smith & Nephew, Inc. Endoscopy Division |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 18, 2008 |
| 510(k) numbers | K034012 |
| FEI number | 3003604053 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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