Device recall
Z-0569-03: Hip Prosthesis as a component of TriFix J Cemented Hip. (Manufactured for…
FDA device recall · Class II · Ortho Development Corporation
Key facts
| Recall number (Z-number) | Z-0569-03 |
|---|---|
| Recall event | 25395 |
| Product | Hip Prosthesis as a component of TriFix J Cemented Hip. (Manufactured for distribution in Japan only.) |
| Recalling firm | Ortho Development Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2003 |
| FEI number | 3017298928 |
At a glance
- None 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