Device recall
Z-2810-2015: Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
FDA device recall · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-2810-2015 |
|---|---|
| Recall event | 71754 |
| Product | Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component |
| Product code | LPH |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2017 |
| 510(k) numbers | K033716 |
| FEI number | 3003070421 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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