Device recall
Z-1073-2009: Dual Taper Wedge Pressed Fit Femoral Component. The Dual Taper Wedge is a single…
FDA device recall · Class II · Stelkast Co
Key facts
| Recall number (Z-number) | Z-1073-2009 |
|---|---|
| Recall event | 50520 |
| Product | Dual Taper Wedge Pressed Fit Femoral Component. The Dual Taper Wedge is a single use device intended for pressed fit reconstruciton of the femoral portion of severely disable and/or very painful hip joints resulting from osteoarthritis, rheumatoid arthritis, traumatic, arthritis or avascular… |
| Product code | LWJ |
| Recalling firm | Stelkast Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 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