Device recall
Z-1537-06: Medtronic 3778 Lead Kit, 1x8 Compact Low Impedance Lead Kit for Spinal Cord…
FDA device recall · Class III · Medtronic Neurological
Key facts
| Recall number (Z-number) | Z-1537-06 |
|---|---|
| Recall event | 36164 |
| Product | Medtronic 3778 Lead Kit, 1x8 Compact Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at: Medtronic, Inc., Villalba, Puerto Rico USA. Medtronic, Inc., Minneapolis, MN 55432-5604. |
| Product code | LGW |
| Recalling firm | Medtronic Neurological |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 31, 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