Device recall
Z-0013-06: TC-PLUS Tibial Insert Ultra-Congruent Size 10; 9 mm, Model 25456
FDA device recall · Class II · Plus Orthopedics USA
Key facts
| Recall number (Z-number) | Z-0013-06 |
|---|---|
| Recall event | 32882 |
| Product | TC-PLUS Tibial Insert Ultra-Congruent Size 10 ; 9 mm, Model 25456 |
| Product code | JWH |
| Recalling firm | Plus Orthopedics USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 16, 2006 |
| 510(k) numbers | K000666 |
| FEI number | 3001237832 |
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