Attune Knee Implant System and Remember
To enhance stability and range of movement in patients needing knee replacement operation, the Attune Knee System medical apparatus was created by DePuy Synthes.if you want to know more about Depuy attune knee lawsuit then you can pop over to www.depuykneelawsuit.com/depuy-knee-recalls.aspx.
But, instead of solving the problems, these devices are connected to complaints from implant recipients that have experienced pain and early device failure leading to the necessity for revision surgery, among other severe issues.
The U. S. FDA (Food and Drug Administration) declared a Class II recall of this DePuy Attune knee augmentation in 2015. This recall was caused by reported temporary or medically reversible bad health problems brought on by this Attune knee augmentation. That remember has been terminated, however, the Attune Knee Implants are still experiencing difficulties.
Attune Knee System Infection
Few of the complications that can detract from your Attune® Knee System are:
- Reduced range of movement
- Fracture of apparatus components or alloy shedding debris
- Loosening or instability of the augmentation
- Heat or heat at the knee or Illness
- Tibial subsidence
- Swelling around the knee joint
- Joint pain and Nerve harm
- Fracture of the femur or tibia
- Apparatus dislocation
- Misalignment of augmentation parts
- Clicking or grinding noises when walking
- The need for revision operation