Device recall
Z-0861-06: Medtronic Kinetra 7428. Dual Program Neurostimulator for Deep Brain Stimulation…
FDA device recall · Class III · Medtronic Neurological
Key facts
| Recall number (Z-number) | Z-0861-06 |
|---|---|
| Recall event | 35110 |
| Product | Medtronic Kinetra 7428. Dual Program Neurostimulator for Deep Brain Stimulation. Rx only. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. Kinetra neurostimulator is a component of the Activa System. The Medtronic Activa System is an implantable, multiprogrammable system that… |
| Product code | MHY |
| Recalling firm | Medtronic Neurological |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 26, 2006 |
| 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