Device recall
Z-2796-2020: Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical…
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-2796-2020 |
|---|---|
| Recall event | 85982 |
| Product | Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wires to… |
| Product code | LRO |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2022 |
| FEI number | 3010667733 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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