How come there a DePuy Leg Replacement Lawsuit?

The DePuy Synthes Attune Leg System was initially introduced this year 2010 as a tool that could improve patient results for total arthroplasty to revive the function of the bones in the leg.

DePuy Synthes, a subsidiary of Johnson & Johnson, promoted these devices as having “patented solutions” that significantly improve range and action and offer patients “the self-assurance of a well balanced knee replacing.” However, a large number of reviews have been submitted with the U.S. Food and Medication Administration (FDA) describing early failures of the Attune(C) Leg System.

A large number of patients have been implanted with the Attune(C) Leg System, a lot of whom have observed premature failing that triggered symptoms such as:

  • Instability and loosening
  • Bloating in the knee
  • Infection
  • Inflammation
  • Bone or muscle damage
  • Reduced range and motion
  • Continuous pain

Oftentimes, the one effective solution for patients who experience a faulty Attune Leg System is to endure a revision surgery to eliminate these devices and replace it. You can get information about the depuy attune knee lawsuit via

Study Sees DePuy Leg Systems are inclined to Failure

In the 2017 study released in the Journal of Leg Surgery, nine orthopedic doctors claim that they had learned a “higher rate of debonding of tibial implant-cement user interface” in the DePuy leg substitution system, which probably induced significant instability in patients.

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