Device recall
Z-0799-2020: Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver…
FDA device recall · Class II · Trilliant Surgical, LLC
Key facts
| Recall number (Z-number) | Z-0799-2020 |
|---|---|
| Recall event | 84350 |
| Product | Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal. |
| Product code | HXX |
| Recalling firm | Trilliant Surgical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 16, 2022 |
| FEI number | 3007420745 |
At a glance
- None 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