Device recall
Z-1059-2012: ENDURAMESH CORPECTOMY SPACER SYSTEM 013MM, 017MM, 023MM by varying heights…
FDA device recall · Class II · Lucero Medical LLC
Key facts
| Recall number (Z-number) | Z-1059-2012 |
|---|---|
| Recall event | 60972 |
| Product | ENDURAMESH CORPECTOMY SPACER SYSTEM 013MM, 017MM, 023MM by varying heights. Dist. By: Lucero Medical, PO Box 67, Richfield, Ohio 44826 Product Usage: Device Description: The Enduramesh is a vertebral body replacement system which provides structural support of the vertebral bodies following an… |
| Product code | MQP |
| Recalling firm | Lucero Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 11, 2014 |
| FEI number | 3008775608 |
At a glance
- None 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