Device recall
Z-0901-03: Trident Insert Impactor
FDA device recall · Class II · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-0901-03 |
|---|---|
| Recall event | 26267 |
| Product | Trident Insert Impactor |
| Product code | HWA |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2003 |
| FEI number | 3003070421 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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