Device recall
Z-0335-2011: Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A. Method of…
FDA device recall · Class II · Medtronic, Inc. - Neuromodulation
Key facts
| Recall number (Z-number) | Z-0335-2011 |
|---|---|
| Recall event | 57024 |
| Product | Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A. Method of Sterilization: Ethylene Oxide. Manufacturer Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The Medtronic Model 8598A Spinal Segment Revision Kit is used when a revision to the spinal segment of a… |
| Product code | LKK |
| Recalling firm | Medtronic, Inc. - Neuromodulation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2011 |
| PMA numbers | P8600004 |
| 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