Device recall
Z-0719-04: Restoration Hip system Cylindrical Distal Extension. Catalog Numbers 1212-3105…
FDA device recall · Class II · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-0719-04 |
|---|---|
| Recall event | 28405 |
| Product | Restoration Hip system Cylindrical Distal Extension. Catalog Numbers 1212-3105, 1212-3115, 1212-3125, and 1212-3195. Sizes 12.5mm, 11.5mm, 19.5mm, and 10.5mm extensions. |
| Product code | LXH |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 9, 2004 |
| FEI number | 3003070421 |
At a glance
- None 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