Device recall
Z-0443-2008: Excia Cemented Hip Stems, Size 16mm, Part Number NJ316K, Aesculap Implant…
FDA device recall · Class II · Aesculap Implant Systems
Key facts
| Recall number (Z-number) | Z-0443-2008 |
|---|---|
| Recall event | 45456 |
| Product | Excia Cemented Hip Stems, Size 16mm, Part Number NJ316K, Aesculap Implant Systems, Inc., Center Valley, PA 18034 |
| Product code | LWJ |
| Recalling firm | Aesculap Implant Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2008 |
| 510(k) numbers | K042344 |
| FEI number | 2916714 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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