Device recall
Z-0290-2007: Medtronic Kinetra Dual Program Neurostimulator for Deep Brain Stimulation, model…
FDA device recall · Class II · Medtronic Neurological
Key facts
| Recall number (Z-number) | Z-0290-2007 |
|---|---|
| Recall event | 35967 |
| Product | Medtronic Kinetra Dual Program Neurostimulator for Deep Brain Stimulation, model 7428. Rx only. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The dual program model 7428 Kinetra Neurostimulator generates electrical signals that are transmitted to the brain. These signals… |
| Product code | MHY |
| Recalling firm | Medtronic Neurological |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2007 |
| PMA numbers | P960009, P960009S027 |
| FEI number | 2182207 |
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