Device recall
Z-2156-2008: Medtronic Midas Rex Legend tapered dissecting tool, Model F2/8TA23 Medtronic…
FDA device recall · Class II · Medtronic Powered Surgical Solutions
Key facts
| Recall number (Z-number) | Z-2156-2008 |
|---|---|
| Recall event | 48472 |
| Product | Medtronic Midas Rex Legend tapered dissecting tool, Model F2/8TA23 Medtronic Powered Surgical Solutions, Forth Worth, TX Intended for use in Spinal, Cranial, Orthopedic, General Surgical and Plastic Surgery applications for transection, osteotomy, graft harvesting, bone shaping, laminectomy, entry… |
| Product code | HBB |
| Recalling firm | Medtronic Powered Surgical Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2009 |
| 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