Device recall
Z-0208-2007: Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is…
FDA device recall · Class II · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-0208-2007 |
|---|---|
| Recall event | 36845 |
| Product | Pioneer Catheter (Crosspoint TransAccess Catheter); Model TA-XP-001; Product is manufactured and distributed by Medtronic Vascular, Santa Rosa, CA 95403 |
| Product code | ITX |
| Recalling firm | Medtronic Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 5, 2007 |
| 510(k) numbers | K031920 |
| FEI number | 3003311129 |
At a glance
- 1–9 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