Device recall
Z-0017-04: TC-PLUS Solution Tibial Component-- Symmetric
FDA device recall · Class II · Plus Endoprothetik AG
Key facts
| Recall number (Z-number) | Z-0017-04 |
|---|---|
| Recall event | 26326 |
| Product | TC-PLUS Solution Tibial Component-- Symmetric |
| Recalling firm | Plus Endoprothetik AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 3, 2003 |
| 510(k) numbers | K000666 |
| FEI number | 3002807898 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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