Device recall
Z-0308-04: EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for…
FDA device recall · Class III · Heartport Inc
Key facts
| Recall number (Z-number) | Z-0308-04 |
|---|---|
| Recall event | 27410 |
| Product | EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients undergoing cardiopulmonary bypass. The EndoReturn cannula with hemostasis valve allows for hemostatic introduction and removal of the Heartport EndoClamp aortic catheter. EndoReturn arterial cannula, 23 Fr… |
| Product code | DWF |
| Recalling firm | Heartport Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 19, 2005 |
| 510(k) numbers | K955121, K971291, K972570, K974736 |
| FEI number | 3000719637 |
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