Device recall
Z-0192-2007: UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26014 Femoral Component…
FDA device recall · Class II · Plus Orthopedics USA
Key facts
| Recall number (Z-number) | Z-0192-2007 |
|---|---|
| Recall event | 36237 |
| Product | UC-PLUS Solution Unicondylar Knee System, Model Numbers: 26014 Femoral Component Size 4, 26016 Femoral Component Size 6, 26018 Femoral Component Size 8 and 26020 Femoral Component Size 10 |
| Product code | HRY |
| Recalling firm | Plus Orthopedics USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2007 |
| 510(k) numbers | K032052 |
| FEI number | 3001237832 |
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