Device recall
Z-1637-2016: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw…
FDA device recall · Class II · Bradshaw Medical Inc.
Key facts
| Recall number (Z-number) | Z-1637-2016 |
|---|---|
| Recall event | 73873 |
| Product | Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a reusable surgical instrument designed to limit the magnitude of applied (input) torque transferred to an external (output) device or fastener in the clockwise direction. The device is… |
| Product code | HXC |
| Recalling firm | Bradshaw Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2020 |
| FEI number | 3006846753 |
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