The Attune knee process is a synthetic medical item made by DePuy Synthes, a subsidiary of Jonson & Johnson healthcare firm. DePuy is your second-largest knee implant producer in the world and is responsible for 38 percent of all hip and knee devices remembered between 2003 and 2013.
Knee and hip replacement devices are known for their regular recalls and higher failure rates before, however, the Attune knee method has been meant to alter all that. If you want to know more about Depuy knee replacement then you can hop over to http://www.depuykneelawsuit.com/depuy-knee-recalls.aspx.
The device was originally sold from the U.S. market in 2010 as a new kind of implant made to enhance joint motion with greater stability.
But as the device was initially introduced into the current market, a lot of patients have complained of device failures and other severe complications. These complaints to the FDA resulted in numerous recalls.
Recognizing the Problem
Most knee implants operate in precisely the exact same manner. A prosthetic joint replaces the knee. So as to do so, the implant has to stick to the leg, usually with a particular kind of adhesive.
Negative side effects of this implant comprising:
- Loosening or instability of the augmentation
- Joint inflammation
- Joint pain
- Nerve harm
- Infection of the joint
- Implant fracturing
- Fracture of the femur or tibia
- Apparatus dislocation
- Tibial subsidence
- The release of metal fragments into the body in the augmentation apparatus
- Misalignment of augmentation parts resulting in grinding
- The decline in range of movement