Device recall
Z-1692-2017: UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical…
FDA device recall · Class II · United Orthopedic Corporation
Key facts
| Recall number (Z-number) | Z-1692-2017 |
|---|---|
| Recall event | 76540 |
| Product | UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral components and femoral trial, and to remove femoral trial. |
| Product code | LXH |
| Recalling firm | United Orthopedic Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2017 |
| FEI number | 1000395711 |
At a glance
- None 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