Device recall
Z-1793-2012: Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product…
FDA device recall · Class II · Aesculap Implant Systems
Key facts
| Recall number (Z-number) | Z-1793-2012 |
|---|---|
| Recall event | 61332 |
| Product | Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Columbus Revision Knee System is indicated for use in reconstruction of the diseased knee joint caused by osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, the need to revise failed… |
| Product code | JWH |
| Recalling firm | Aesculap Implant Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 15, 2014 |
| 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