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FDA Issues Most Serious Recall Classification After Software Error in Automated Impella Controllers Linked to Reported Injuries and Death What Parker Waichman …

Johnson & Johnson’s Abiomed has issued another safety correction involving Automated Impella Controllers, the devices used to control and monitor Impella heart …

A Sharp Rise in Class I Medical Device Recalls Highlights Growing Risks for Patients Harmed by Defective Medical Devices What Parker Waichman …

Johnson & Johnson MedTech Recall Raises Concerns About Blood Clot Formation, Vascular Complications, and Patient Safety During Critical Heart Procedures What Parker …

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 …