Device recall
Z-0568-03: Hip Prosthesis as a component of Primaloc Cemented Hip System.
FDA device recall · Class II · Ortho Development Corporation
Key facts
| Recall number (Z-number) | Z-0568-03 |
|---|---|
| Recall event | 25395 |
| Product | Hip Prosthesis as a component of Primaloc Cemented Hip System. |
| Recalling firm | Ortho Development Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2003 |
| 510(k) numbers | K962448 |
| FEI number | 3017298928 |
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