Device recall
Z-0375-2010: Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, standard…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-0375-2010 |
|---|---|
| Recall event | 52806 |
| Product | Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, standard, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-001-00. The device is used to drill into the proximal tibia or distal femur for placement of screws that stabilize the position of an intramedullary nail implant. The targeting… |
| Product code | HSB |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2011 |
| 510(k) numbers | K082770, K083497, K090596 |
| FEI number | 1000220733 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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