Device recall
Z-0556-05: The Triathlon Posteriorly Stabilized Femoral Component.
FDA device recall · Class III · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-0556-05 |
|---|---|
| Recall event | 30379 |
| Product | The Triathlon Posteriorly Stabilized Femoral Component. |
| Product code | NPJ |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 31, 2005 |
| FEI number | 3003070421 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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