Device recall
Z-1415-06: Medtronic Intrathecal Catheter Distal Revision Kit, Model 8598, (provides…
FDA device recall · Class I · Medtronic Neurological
Key facts
| Recall number (Z-number) | Z-1415-06 |
|---|---|
| Recall event | 35931 |
| Product | Medtronic Intrathecal Catheter Distal Revision Kit, Model 8598, (provides replacement parts for the distal section of the 8731 Intrathecal Catheter) . 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