DePuy Synthes ATTUNE® Knee Recall

If you suffered painful side effects after having a DePuy Synthes ATTUNE® Knee Implant, call (877) 562-0000 to find out if you qualify for compensation.

ATTUNE® Knee Implant Side Effects

Injuries such as Tibial Loosening can occur if an ATTUNE® knee implant fails. A patient can suffer painful side effects or require additional surgeries.

Symptoms of ATTUNE® Knee Implant Failure May Include:

  • Joint loosening or dislocation
  • Knee pain
  • Loss of range of motion

FDA Recalls ATTUNE® Knee Implant

DePuy, a division of Johnson & Johnson, recalled the ATTUNE® Knee Implant because of problems reported with a spring that can come loose from the device and become lodged in the patient’s body. According to the Food and Drug Administration (FDA) approximately 3,500 ATTUNE® Knee Implants have been recalled. The ATTUNE® knee implant device failure causes an injury known as Tibial Loosening.

You May Qualify For Compensation If:

  • You had a DePuy ATTUNE® knee appliance implanted after Feb. 13, 2015
  • Required revision surgery to replace the implant

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Call (877) 562-0000 or fill out our online form for a FREE legal consultation.

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At Cory Watson Attorneys, we have made it our mission to fight for the rights of injury victims and their families for over 30 YEARS, and have recovered more than $2.7 BILLION for clients.


Cory Watson Attorneys is not affiliated with the FDA, DePuy or Johnson & Johnson