Attune Knee Replacement Failure

DePuy Synthesis markets that the Attune Knee System as using “patented technology” that enhance range of movement and provide patients “the assurance of a secure knee replacement.”

Nonetheless, in recent decades, DePuy synthesis has registered dozens of reports together with the Food and Drug Administration Assessing early failures of this Attune Knee System which have caused the destabilization of patients’ knee replacements and debilitating revision surgeries. If you want to know more about lawsuits for defective Depuy knee replacement systems then click right here.

DePuy Knee Revision Surgery

In addition, in an article published in the Journal of Knee Surgery, many notable orthopedic surgeons reported they have struck an unusually large rate of early failures of their Attune Knee System. The surgeons blamed the failures into the debonding of the tibial implant-cement interface.

Countless individuals have been implanted with the Attune® Knee System. Symptoms Related to early failures of this Attune® Knee System include:

  • Instability and Loosening
  • Unusual Swelling
  • Reduced Range of Motion
  • Persistent Pain

Typically, the sole medical option for patients who undergo a premature collapse of the Attune® Knee System is to experience a revision operation to remove the implant and replace it. These contraceptive surgeries are often more painful and debilitating than the first replacement operation.

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