Device recall
Z-1261-2009: Zimmer Sirus Intramedullary nail for tibia, cannulated, diameter 12 L, 330 mm…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-1261-2009 |
|---|---|
| Recall event | 51687 |
| Product | Zimmer Sirus Intramedullary nail for tibia, cannulated, diameter 12 L, 330 mm, sterile, Zimmer GmbH, Winterthur, Switzerland; REF 02.02631.233. The device is used in orthopedic trauma surgeries for stabilization of tibial bone fractures. |
| Product code | HSB |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2009 |
| 510(k) numbers | K043270 |
| 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