Device recall
Z-0700-2007: The Precision Implantable Pulse Generator, Model Number SC-1110
FDA device recall · Class III · Advanced Bionics Corp
Key facts
| Recall number (Z-number) | Z-0700-2007 |
|---|---|
| Recall event | 37462 |
| Product | The Precision Implantable Pulse Generator, Model Number SC-1110 |
| Product code | LGW |
| Recalling firm | Advanced Bionics Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 25, 2012 |
| PMA numbers | P030017 |
| FEI number | 1000220815 |
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