Device recall
Z-2456-2015: Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20…
FDA device recall · Class II · Trilliant Surgical Ltd.
Key facts
| Recall number (Z-number) | Z-2456-2015 |
|---|---|
| Recall event | 71815 |
| Product | Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20 mm; Concave Reamer Head 22 mm; Convex Reamer Head, 16 mm; Convex Reamer Head, 18 mm; Convex Reamer Head 20 mm; Convex Reamer Head 22 mm, used with Gridlock Plating system, for use in trauma and reconstructive procedures… |
| Product code | HTO |
| 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
- 10–99 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