Device recall
Z-1926-2008: Medtronic Select 3D and Select CAP Aterial Cannulae with flexible, thin wall…
FDA device recall · Class II · Medtronic Perfusion Systems
Key facts
| Recall number (Z-number) | Z-1926-2008 |
|---|---|
| Recall event | 48100 |
| Product | Medtronic Select 3D and Select CAP Aterial Cannulae with flexible, thin wall wire-wound PVC bodies with angled, beveled tips. Catalog Number: CB78722 |
| Product code | DWF |
| Recalling firm | Medtronic Perfusion Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| 510(k) numbers | K033416 |
| FEI number | 1000116158 |
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