Device recall
Z-0499-2009: FC400SP microTargeting StimPilot Single Procedure Kit Distributed by Medtronic…
FDA device recall · Class II · FHC, Inc.
Key facts
| Recall number (Z-number) | Z-0499-2009 |
|---|---|
| Recall event | 50103 |
| Product | FC400SP microTargeting StimPilot Single Procedure Kit Distributed by Medtronic Inc., Minneapolis, MN Ref: FHC4000SP Intended for use in intra-operative recording of single unit neuronal activity or intra-operative stimulation of neural elements in the brain. |
| Product code | GZL |
| Recalling firm | FHC, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2012 |
| 510(k) numbers | K991522 |
| FEI number | 3002250546 |
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