If you are thinking to undergo a knee replacement, this article is just for you.
The Food and Drug Administration (FDA) has been getting an uptick in grievances from new patients of knee replacement surgeries, explicitly from those who have already undergone DePuy knee replacement or Depuy Attune Knee Replacement surgery.
Well, you will be surprised to know that in a very short span of time, Lawsuits for Defective DePuy Knee Replacement have been filed, frequently.
Now, situation has reached to this level that lots of patients are wondering or I would say waiting for legal DePuy knee replacement recall.
But what exactly happened that patients want this to be recalled from the market.
Problems With the DePuy Synthes Knee Replacement
The complaints and claims received by the FDA about this knee placement system have inclined to center around the device’s catastrophe to permit for contented and robust use.
Regardless of offering safe and comfortable firmness to the patients, a lot of people mentioned that experienced problems for weeks or a few months after their surgery, expressing they experienced serious pain, loosening, and unpredictable balance on the knee and calf.
Due to these reasons, people started to demand for immediate depuy knee recall.
Furthermore, issues such as muscle destruction, bone damage, and an infection become serious problems for the patients.
Oftentimes, the only path to repair the symptoms induced by this new replacing system was to have duplicate intrusive surgery.
This additional surgery was equally as highly intrusive as the original knee replacement unit surgery and induced a lengthy restoration period as well as additional pain, soreness, and struggling for the patients.
(Do find out more about the lawsuits filed and what sort of actions has been taken yet in regards to all of these lawsuits online.)
Finally, a few of the damage these malfunctioning knee substitute implants triggered with completely irreversible.