Device recall
Z-0664-2009: Stelkast Dual Taper Wedge Pressed Fit Femoral Component. Hip Prosthesis, Part…
FDA device recall · Class II · Stelkast Co
Key facts
| Recall number (Z-number) | Z-0664-2009 |
|---|---|
| Recall event | 50128 |
| Product | Stelkast Dual Taper Wedge Pressed Fit Femoral Component. Hip Prosthesis, Part number SC1439 |
| Product code | LWJ |
| Recalling firm | Stelkast Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2009 |
| 510(k) numbers | K953268 |
| FEI number | 3004142400 |
At a glance
- 1–9 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