Device recall
Z-0489-2007: LCP Volar Distal Radius Plate Extra Articular 4H HD-RT-Long, LCP Volar Distal…
FDA device recall · Class II · Synthes
Key facts
| Recall number (Z-number) | Z-0489-2007 |
|---|---|
| Recall event | 37010 |
| Product | LCP Volar Distal Radius Plate Extra Articular 4H HD-RT-Long, LCP Volar Distal Radius Plate 2.4 mm, Catalog number 242.465 |
| Product code | HRS |
| Recalling firm | Synthes |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 13, 2007 |
| 510(k) numbers | K012114 |
| FEI number | 3005180112 |
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