Device recall
Z-0960-2008: Advanced Bionics Precision Implantable Pulse Generator Kit, Model Number…
FDA device recall · Class II · Advanced Bionics Corp
Key facts
| Recall number (Z-number) | Z-0960-2008 |
|---|---|
| Recall event | 45853 |
| Product | Advanced Bionics Precision Implantable Pulse Generator Kit, Model Number: SC-1110 with firmware version prior to Revision 3.02, Advanced Bionics Corportation, Sylmar, CA 91342 |
| Product code | LGW |
| Recalling firm | Advanced Bionics Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 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