Device recall
Z-0278-05: Medtronic Midas Rex Legend High Speed Pneumatic System
FDA device recall · Class II · Power Surgical Solutions
Key facts
| Recall number (Z-number) | Z-0278-05 |
|---|---|
| Recall event | 30509 |
| Product | Medtronic Midas Rex Legend High Speed Pneumatic System |
| Product code | HBB |
| Recalling firm | Power Surgical Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 20, 2005 |
| 510(k) numbers | K020069 |
| FEI number | 1625507 |
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