Device recall
Z-2159-2018: Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector…
FDA device recall · Class II · Maquet Cardiopulmonary Ag
Key facts
| Recall number (Z-number) | Z-2159-2018 |
|---|---|
| Recall event | 80076 |
| Product | Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number A20-0101. For use in cardiopulmonary bypass |
| Product code | DWF |
| Recalling firm | Maquet Cardiopulmonary Ag |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2020 |
| 510(k) numbers | K012774 |
| FEI number | 3009507273 |
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