If you or someone you love has suffered from a faulty knee replacement using Aesculap models listed below, please contact us today using our confidential form located on this page.
The four models below have been medically proven to be a faulty replacement with a high probability of requiring immediate replacement:
- VEGA Knee System
- Columbus Knee System
- Univation X
- EnduRo A S Knee Revision System
In November 2015, Aesculap Inc initiated a recall on Tibial and Femur extension sterile pressfit stem implant packaging that are used in the Columbus Revision and EnduRo Knee Implants because it is labeled as Cementless, when the US product has been indicated for use with Bone Cement only. Aesculap has also been in multiple lawsuits for their failing IVC filter as well.
Find Out If You Qualify Today
To find out if you qualify to file a knee replacement lawsuit regarding an Aesculap knee implant, please contact us today. Principal Law Group attorneys are in the process of investigating faulty replacements for anyone who believe they may have a claim. To learn more, simply fill out the contact form and we will be in touch with you shortly.