Device recall
Z-1447-2014: K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is…
FDA device recall · Class II · Breg Inc
Key facts
| Recall number (Z-number) | Z-1447-2014 |
|---|---|
| Recall event | 67821 |
| Product | K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is intended to provide flexible knee support. |
| Product code | IQI |
| Recalling firm | Breg Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2014 |
| FEI number | 1000125378 |
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