Device recall
Z-0814-2018: OTTO BOCK Kenevo knee joints Model 3C60
FDA device recall · Class II · Otto Bock Healthcare Product
Key facts
| Recall number (Z-number) | Z-0814-2018 |
|---|---|
| Recall event | 79019 |
| Product | OTTO BOCK Kenevo knee joints Model 3C60 |
| Product code | ISY |
| Recalling firm | Otto Bock Healthcare Product |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2021 |
| FEI number | 3005190268 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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