Device recall
Z-1602-2016: Medtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use…
FDA device recall · Class II · Medtronic Sofamor Danek Usa, Inc - Dallas Distribution
Key facts
| Recall number (Z-number) | Z-1602-2016 |
|---|---|
| Recall event | 73869 |
| Product | Medtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use in neurosurgery. |
| Product code | HBB |
| Recalling firm | Medtronic Sofamor Danek Usa, Inc - Dallas Distribution |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2017 |
| 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