Device recall
Z-2368-2012: Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral…
FDA device recall · Class II · Lucero Medical LLC
Key facts
| Recall number (Z-number) | Z-2368-2012 |
|---|---|
| Recall event | 62926 |
| Product | Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral body replacement system intended for use in the thoracic and lumbar spine (T1-S1) to replace a collapsed, damaged or unstable vertebral body due to tumor or trauma/fracture. The device is intended for use with either… |
| Product code | MQP |
| Recalling firm | Lucero Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2013 |
| 510(k) numbers | K093207 |
| FEI number | 3008775608 |
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