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.


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