Device recall
Z-0571-04: Restoration T3 Revision Hip System, Femoral Hip Prosthesis. Various lengths and…
FDA device recall · Class II · Stryker Howmedica Osteonics
Key facts
| Recall number (Z-number) | Z-0571-04 |
|---|---|
| Recall event | 28052 |
| Product | Restoration T3 Revision Hip System, Femoral Hip Prosthesis. Various lengths and Model numbers. 6260-3-014 T3 MOD REV DIST STM 14MMX225MM; 6260-3-015 T3 MOD REV DIST STM 15MMX225MM; 6260-3-016 T3 MOD REV DIST STM 16MMX225MM; 6260-3-017 T3 MOD REV DIST STM 17MMX225MM; 6260-3-018 T3 MOD REV DIST STM… |
| Product code | LZO |
| Recalling firm | Stryker Howmedica Osteonics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2006 |
| 510(k) numbers | K013106, K983404 |
| 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