Device recall
Z-0786-2022: Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF…
FDA device recall · Class II · Wright Medical Technology, Inc.
Key facts
| Recall number (Z-number) | Z-0786-2022 |
|---|---|
| Recall event | 89507 |
| Product | Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System. |
| Product code | HRS |
| Recalling firm | Wright Medical Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2022 |
| 510(k) numbers | K090692 |
| FEI number | 3010667733 |
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