Device recall
Z-2300-2008: Zimmer M/G Unicompartmental Knee System headed screw, 48 mm length, sterile…
FDA device recall · Class III · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-2300-2008 |
|---|---|
| Recall event | 48716 |
| Product | Zimmer M/G Unicompartmental Knee System headed screw, 48 mm length, sterile, Catalog No. 00-5791-041-00. Used during surgery for the cutting guide. This screw is not permanently implanted. |
| Product code | LXH |
| Recalling firm | Zimmer Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 17, 2008 |
| FEI number | 1000220733 |
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