Device recall
Z-0663-2018: NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral…
FDA device recall · Class II · ZIMMER ORTHOPEDIC MFG LTD
Key facts
| Recall number (Z-number) | Z-0663-2018 |
|---|---|
| Recall event | 78960 |
| Product | NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral condyle of the knee joint in Total Knee Arthroplasty. |
| Product code | NJL |
| Recalling firm | ZIMMER ORTHOPEDIC MFG LTD |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 16, 2018 |
| PMA numbers | P060037 |
| FEI number | 3007963827 |
At a glance
- None 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