Device recall
Z-1247-2016: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip…
FDA device recall · Class II · Neurotherm, Inc.
Key facts
| Recall number (Z-number) | Z-1247-2016 |
|---|---|
| Recall event | 73407 |
| Product | Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue in the human body for pain… |
| Product code | GXI |
| Recalling firm | Neurotherm, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 25, 2016 |
| 510(k) numbers | K000073 |
| FEI number | 3002953813 |
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