Device recall
Z-1723-2015: Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesis…
FDA device recall · Class II · Vilex In Tennessee Inc
Key facts
| Recall number (Z-number) | Z-1723-2015 |
|---|---|
| Recall event | 71344 |
| Product | Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis. |
| Product code | HSB |
| Recalling firm | Vilex In Tennessee Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 30, 2016 |
| 510(k) numbers | K102413 |
| FEI number | 1051526 |
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