Device recall
Z-1381-2008: Scorpio Total Knee Cruciate Retraining Femoral Component; Knee joint…
FDA device recall · Class III · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-1381-2008 |
|---|---|
| Recall event | 47219 |
| Product | Scorpio Total Knee Cruciate Retraining Femoral Component; Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis; Product Number: 70-300-7R; Stryker Corp, Howmedica Osteonics Corp, Mahwah, NJ 07430. |
| Product code | JWH |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 16, 2008 |
| 510(k) numbers | K974556 |
| 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