Device recall
Z-1482-2009: Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 00…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-1482-2009 |
|---|---|
| Recall event | 51406 |
| Product | Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 00, for cemented use only, sterile, Zimmer, Warsaw, IN; Model Number: 6420-00-002. The Natural-Knee II System Cemented Modular Tibial Baseplate is a nonporous component which may be used in total knee replacement surgery… |
| Product code | JWH |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2009 |
| 510(k) numbers | K023528 |
| FEI number | 1000220733 |
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