Device recall
Z-1140-2020: NC TRAVELER Coronary Dilatation Catheter, REF 1013157-08, Rx Only,NC Traveler RX…
FDA device recall · Class I · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-1140-2020 |
|---|---|
| Recall event | 84826 |
| Product | NC TRAVELER Coronary Dilatation Catheter, REF 1013157-08, Rx Only,NC Traveler RX 4.0 X 8MM The NC Traveler RX Coronary Dilatation Catheter is not cleared for commercial distribution in the United States. |
| Product code | LOX |
| Recalling firm | Abbott Vascular |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 16, 2024 |
| 510(k) numbers | K103153, K110134 |
| FEI number | 2024168 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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