Device recall
Z-1706-2012: Stryker Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-1706-2012 |
|---|---|
| Recall event | 61766 |
| Product | Stryker Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number 48237026. Product Usage: : Reusable instrument used to aid in the final tightening of the spinal construct. Intended Use: The Anti-Torque Key allows the Torque Wrench to align with the tightening axis and maximizing the torque… |
| Product code | NKB |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2013 |
| 510(k) numbers | K071373 |
| FEI number | 3004024955 |
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