Device recall
Z-1869-2009: Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating…
FDA device recall · Class II · Maquet Cardiovascular
Key facts
| Recall number (Z-number) | Z-1869-2009 |
|---|---|
| Recall event | 52663 |
| Product | Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating balloon tip or cone distal tips, straight or right angle, available with proximal end fittings for either 1/4 inch connector or male luer fitting, Model numbers 210800, 210801, 210802, 210803, 210804, 210805, 210806… |
| Product code | DWF |
| Recalling firm | Maquet Cardiovascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2010 |
| FEI number | 3000719698 |
At a glance
- None 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