Device recall
Z-1414-06: Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using…
FDA device recall · Class I · Medtronic Neurological
Key facts
| Recall number (Z-number) | Z-1414-06 |
|---|---|
| Recall event | 35931 |
| Product | Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using Medtronic implantable pumps) The catheter is designed for use in the intrathecal space. Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. |
| Product code | LKK |
| Recalling firm | Medtronic Neurological |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 21, 2007 |
| PMA numbers | P860004 |
| FEI number | 2182207 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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