Device recall
Z-0546-2010: Medtronic Midas Rex Legend Footed Attachment, AF01. Intended for use with all…
FDA device recall · Class II · Medtronic Sofamor Danek Usa, Inc - Dallas Distribution
Key facts
| Recall number (Z-number) | Z-0546-2010 |
|---|---|
| Recall event | 53996 |
| Product | Medtronic Midas Rex Legend Footed Attachment, AF01. Intended for use with all Legend and Legend EHS motors for general surgery including maxillofacial , craniofacial and sternotomy applications. |
| Product code | HBB |
| Recalling firm | Medtronic Sofamor Danek Usa, Inc - Dallas Distribution |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2010 |
| 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