Device recall
Z-1786-2013: STERIS Fine Traction Device, one unit per box Product Usage: The Fine Traction…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-1786-2013 |
|---|---|
| Recall event | 65573 |
| Product | STERIS Fine Traction Device, one unit per box Product Usage: The Fine Traction Device is used to provide traction and enable fine adjustments to traction and orientation of the leg during orthopedic procedures. |
| Product code | HST |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2013 |
| FEI number | 1527821 |
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