Device recall
Z-0202-2015: GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment…
FDA device recall · Class II · Medacta Usa
Key facts
| Recall number (Z-number) | Z-0202-2015 |
|---|---|
| Recall event | 69493 |
| Product | GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement. |
| Product code | HSB |
| Recalling firm | Medacta Usa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2015 |
| FEI number | 3015500078 |
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