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FDA Class I Recall Involves Certain Relay Pro Thoracic Stent Grafts After Reports of Device Release Failure, Emergency Open Surgery, Stroke, Aortic …

FDA Issues Class I Recall After Reports Of Thousands Of Injuries And Multiple Deaths Linked To Pacemaker Software Problems What Parker Waichman …

Thousands Of Injuries And Multiple Deaths Reported In Connection With ACCOLADE Pacemakers And CRT-P Devices What Parker Waichman LLP Found More than …

Omnipod Insulin Pump Recall Lawsuit: Nearly 30 Serious Injuries Linked To Insulin Underdosing Risk What Parker Waichman LLP Found Defective pods may …

FDA Class I Recall Raises Concerns Over Dangerous Error Code Confusion And Delayed Treatment Risks What Parker Waichman LLP Found: Confusing error …

Heart Pump Recall Lawsuits: HeartMate II And III Heart Pumps Linked To Deaths, Injuries, And Blood Flow Failures What Parker Waichman LLP …

Sharp Increase In High-Risk Device Recalls May Leave Injured Patients With Legal Claims Across The United States What Parker Waichman LLP Found …

Patients and medical staff injured by rupturing cryotherapy probes may have legal options under product liability laws. The U.S. Food and Drug …

Patients and Families May Have Legal Options After the FDA’s Most Serious Recall Classification for Certain CERENOVUS Coil Devices The recall involving …

Patients Harmed by Stent Deployment and Expansion Failures May Have Grounds for a Medical Device Lawsuit FDA Issues Early Alert After Stent …