Device recall
Z-1369-04: P.F.C. Knee System 7 Fluted Femoral Stem 18mmX125mm REF 96-1703
FDA device recall · Class III · Depuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1369-04 |
|---|---|
| Recall event | 29314 |
| Product | P.F.C. Knee System 7 Fluted Femoral Stem 18mmX125mm REF 96-1703 |
| Product code | JWH |
| Recalling firm | Depuy Orthopaedics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 23, 2004 |
| 510(k) numbers | K952830 |
| FEI number | 1818910 |
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