Device recall
Z-1384-04: The Model 8540 Catheter Access Port Kit is intended for use in accessing the…
FDA device recall · Class II · Medtronic Inc, Neurological & Spinal Division
Key facts
| Recall number (Z-number) | Z-1384-04 |
|---|---|
| Recall event | 29663 |
| Product | The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via the catheter access port of Medtronic(R) implantable programmable infusion pumps (except Medtronic MiniMed pumps). The Model 8540 Catheter Access Port Kit does not have a product code for itself; it is approved… |
| Product code | LKK |
| Recalling firm | Medtronic Inc, Neurological & Spinal Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2005 |
| 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