Device recall
Z-0995-2009: Cyberonics VNS Therapy Demipulse Duo Generator, Model 104; an implantable…
FDA device recall · Class III · Cyberonics, Inc
Key facts
| Recall number (Z-number) | Z-0995-2009 |
|---|---|
| Recall event | 47442 |
| Product | Cyberonics VNS Therapy Demipulse Duo Generator, Model 104; an implantable, multiprogrammable, vagus nerve stimulator. |
| Product code | LYJ |
| Recalling firm | Cyberonics, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 28, 2011 |
| PMA numbers | P970003 |
| FEI number | 1000117004 |
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