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FDA Raises Alarm Over Glucose Sensor Accuracy and Patient Safety The U.S. Food and Drug Administration (FDA) has issued an urgent Early …

Over 103,000 Defective Lung Biopsy Devices Pulled From Market Following Reports of Airway Injuries, Component Ejection, and Fatal Complications On September 25, …

FDA Confirms Life-Threatening Safety Mode Malfunction Risk in Boston Scientific’s Accolade Family of Pacemakers The U.S. Food and Drug Administration (FDA) has …

Olympus Recalls ViziShot 2 FLEX Endoscopic Aspiration Needles After Reports of Injuries and Death Medical devices are intended to help diagnose, treat, …

Boston Scientific Defibrillator Lead Recall Raises Alarms Over Shock Failures and Fatal Cardiac Events Thousands of patients across the United States rely …

Boston Scientific Issues Urgent Safety Update Over Increased Risk of Air Embolism During Watchman Implant Procedures The Watchman Access System, developed by …

Understanding the Risks of Defibrillator Wire Failures and Watchman Implant Complications and How Victims Can Seek Justice The U.S. Food and Drug …

Boston Scientific ENDOTAK RELIANCE Defibrillation Lead Alert: Patient Risks, Injuries, and Legal Options The recent FDA Early Alert concerning Boston Scientific’s ENDOTAK …

A recent Class I recall issued by the U.S. Food and Drug Administration (FDA) has brought serious attention to the safety of …

Nationwide Safety Concerns Over Baxter’s Novum IQ Large Volume Pump and Potential Legal Claims for Victims The U.S. Food and Drug Administration …