Device recall
Z-2679-2014: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm…
FDA device recall · Class II · Instratek, Incorporated
Key facts
| Recall number (Z-number) | Z-2679-2014 |
|---|---|
| Recall event | 67727 |
| Product | Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System |
| Product code | HWC |
| Recalling firm | Instratek, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2016 |
| 510(k) numbers | K120493 |
| FEI number | 1000118334 |
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