Device recall
Z-0170-2010: Eon Rechargeable Implantable Pulse Generator (IPG) System
FDA device recall · Class II · Advanced Neuromodulation Systems, Inc
Key facts
| Recall number (Z-number) | Z-0170-2010 |
|---|---|
| Recall event | 53128 |
| Product | Eon Rechargeable Implantable Pulse Generator (IPG) System |
| Product code | LGW |
| Recalling firm | Advanced Neuromodulation Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2010 |
| PMA numbers | P010032, P010032S014 |
| FEI number | 1627487 |
At a glance
- None 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