Device recall
Z-0489-04: Depuy brand ACE trochanteric nail anti-rotation/ superior screw; non-sterile, 5…
FDA device recall · Class II · Depuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-0489-04 |
|---|---|
| Recall event | 27923 |
| Product | Depuy brand ACE trochanteric nail anti-rotation/ superior screw; non-sterile, 5 mm x 80 mm; Product 903005080. |
| Product code | HSB |
| Recalling firm | Depuy Orthopaedics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2004 |
| 510(k) numbers | K010780 |
| FEI number | 1818910 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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