Device recall
Z-2490-2015: 7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY…
FDA device recall · Class II · Trilliant Surgical Ltd.
Key facts
| Recall number (Z-number) | Z-2490-2015 |
|---|---|
| Recall event | 71967 |
| Product | 7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part # 300-60-002 NON-STERILE SINGLE USE ONLY; 11 Hole VL Gridlock Fibula Plate, Part # 300-60-003 NON-STERILE SINGLE USE ONLY. For use in trauma and reconstructive procedures in small… |
| Product code | HRS |
| Recalling firm | Trilliant Surgical Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2017 |
| 510(k) numbers | K121452 |
| 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