Device recall
Z-0480-2008: StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number…
FDA device recall · Class III · Stelkast Co
Key facts
| Recall number (Z-number) | Z-0480-2008 |
|---|---|
| Recall event | 45528 |
| Product | StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number SC2287-2-5, Size 2 Thickness 5 mm, StelKast, Murray, PA 15317 |
| Product code | JWH |
| Recalling firm | Stelkast Co |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 23, 2008 |
| 510(k) numbers | K051976 |
| FEI number | 3004142400 |
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