Device recall
Z-2158-2008: Stem Trial, Triathlon Revision Instruments; Non-Sterile; 150 mm length Catalog…
FDA device recall · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-2158-2008 |
|---|---|
| Recall event | 48596 |
| Product | Stem Trial, Triathlon Revision Instruments; Non-Sterile; 150 mm length Catalog Numbers: 5566-T-009, 5566-T-010, 5566-T-011, 5566-T-012, 5566-T-013, 5566-T-014 5566-T-015, 5566-T-016, 5566-T-017, 5566-T-018, 5566-T-019, 5566-T-020 5566-T-021, 5566-T-022, 5566-T-023, 5566-T-024, 5566-T-025 Howmedica… |
| Product code | HWT |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2010 |
| 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