Device recall
Z-1043-2016: Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus…
FDA device recall · Class II · Aesculap, Inc.
Key facts
| Recall number (Z-number) | Z-1043-2016 |
|---|---|
| Recall event | 72853 |
| Product | Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint. |
| Product code | JWH |
| Recalling firm | Aesculap, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2016 |
| 510(k) numbers | K083772 |
| FEI number | 2916714 |
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