Device recall
Z-2452-2015: 3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System…
FDA device recall · Class II · Trilliant Surgical Ltd.
Key facts
| Recall number (Z-number) | Z-2452-2015 |
|---|---|
| Recall event | 71812 |
| Product | 3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for… |
| Product code | HTW |
| Recalling firm | Trilliant Surgical Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2017 |
| 510(k) numbers | K081510 |
| FEI number | 3007420745 |
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