Device recall
Z-1344-2022: Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ…
FDA device recall · Class II · Abbott
Key facts
| Recall number (Z-number) | Z-1344-2022 |
|---|---|
| Recall event | 90414 |
| Product | Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ, REF A-TCSE-FJ. For mapping of the heart chambers during ablation. |
| Product code | OAE |
| Recalling firm | Abbott |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 14, 2026 |
| PMA numbers | P130026, P130026S036 |
| FEI number | 3005334138 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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