Device recall
Z-0291-2008: Pioneer Quantum Spinal Rod System, MIS Yoke Manipulator, Long Slot, non-sterile…
FDA device recall · Class II · Pioneer Surgical Technology
Key facts
| Recall number (Z-number) | Z-0291-2008 |
|---|---|
| Recall event | 45526 |
| Product | Pioneer Quantum Spinal Rod System, MIS Yoke Manipulator, Long Slot, non-sterile; Cat # 51-YOKEMAN-L, Pioneer Surgical Technology, Marquette, MI 49855 |
| Product code | HWR |
| Recalling firm | Pioneer Surgical Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2008 |
| FEI number | 1000115331 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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