Results for: depuy

DePuy Synthes Elbow

DePuy Synthes Elbow Lawsuit

DePuy Synthes Elbow Replacement linked to dozens of reports of complications including device loosening, osteolysis, poor joint mechanics, bone fractures, soft tissue damage, revision surgery. Manufacturer pulled the Radial Head Prosthesis System off the U.S. market in 2016 after it...

Knee Implant

DePuy Synthes Attune Knee Class Action Lawsuit

Our lawyers are reviewing potential lawsuits for knee replacement patients who suffered complications after receiving a DePuy Synthes Attune knee implant.

Knee Implant

DePuy Synthes Attune Knee Lawsuit

The Attune Knee System, was designed to improve stability and range of motion in knee replacement patients but has been linked to reports of pain and premature implant failure.

depuy-synthes-power-tool-battery-adapter

DePuy Synthes Power Tool Battery Adaptor Lawsuit

The U.S. Food & Drug Administration (FDA) has issued a Class I Recall for about 450 power tool system battery adaptors made by DePuy Synthes over a potential design flaw that may cause the devices to explode, causing serious injury...

DePuy Synthes Craniomaxillofacial (CMF) Distraction System Class Action Lawsuit

DePuy Craniomaxillofacial (CMF) Distraction System Class Action Lawsuit

The DePuy Synthes Craniomaxillofacial (CMF) Distraction System, which is used to correct defects of the jaw, has the potential to reverse direction after surgery, which may result in tracheal obstruction, respiratory arrest or death. To date, at least 15 injuries...

DePuy Synthes Craniomaxillofacial (CMF) Distraction System Class Action Lawsuit

DePuy Craniomaxillofacial Distraction System Lawsuit

Our lawyers are accepting potential lawsuits on behalf of people who were injured by the DePuy Synthes Craniomaxillofacial (CMF) Distraction System. This device, which is used to lengthen or stabilize the jawbone, may reverse direction and lose the desired distraction...

DePuy Knee Replacement Recall Lawsuit

February 22, 2013 - Johnson & Johnson (J&J) is now recalling an orthopedic knee replacement device due to a potential for fractures, the U.S. Food & Drug Administration (FDA) announced today. The LPS Diaphyseal Sleeve, which was manufactured by J&J’s...