Device recall
Z-1382-04: P.F.C. Modular Knee System Modular Plus Tibial Wedge 10 HEMI x 8.5MM HEIGHT…
FDA device recall · Class III · Depuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1382-04 |
|---|---|
| Recall event | 29309 |
| Product | P.F.C. Modular Knee System Modular Plus Tibial Wedge 10 HEMI x 8.5MM HEIGHT Product Code: 86-0178 |
| Product code | JWH |
| Recalling firm | Depuy Orthopaedics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 23, 2004 |
| 510(k) numbers | K923807 |
| 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