Device recall
Z-1250-2010: MaxTorque Cannulated Screw Model # MSD-010-55-060S
FDA device recall · Class II · Orthohelix Surgical Designs Inc
Key facts
| Recall number (Z-number) | Z-1250-2010 |
|---|---|
| Recall event | 54540 |
| Product | MaxTorque Cannulated Screw Model # MSD-010-55-060S |
| Product code | HWC |
| Recalling firm | Orthohelix Surgical Designs Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2010 |
| 510(k) numbers | K060428 |
| FEI number | 3000718467 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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