Device recall
Z-2811-2026: EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as…
FDA device recall · Class II · Medtronic Perfusion Systems
Key facts
| Recall number (Z-number) | Z-2811-2026 |
|---|---|
| Recall event | 99320 |
| Product | EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78322 |
| Product code | DWF |
| Recalling firm | Medtronic Perfusion Systems |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K260195 |
| FEI number | 1000116158 |
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