Device recall
Z-0763-06: Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse…
FDA device recall · Class II · Medtronic Cardiac Surgery Technologies
Key facts
| Recall number (Z-number) | Z-0763-06 |
|---|---|
| Recall event | 33341 |
| Product | Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse. Nonpyrogenic. The SPYDER is designed to create an anastomosis in a rapid, automated fashion. The device creates an interrupted anastomosis without the need for aortic clamping. A specially designed aortic cutting device… |
| Product code | FZP |
| Recalling firm | Medtronic Cardiac Surgery Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2007 |
| 510(k) numbers | K024366, K031623 |
| FEI number | 3003368396 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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