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Understanding the expanded recall of Olympus ViziShot 2 FLEX needles, the risks of detached components during biopsy procedures, and your options for …

What Patients and Families Should Know About the FDA Alert, Reported Injuries, and Potential Legal Claims The U.S. Food and Drug Administration …

Defective Labeling of IV Extension Sets May Lead to Fatal Air Embolism: What Patients and Families Should Know About Their Rights. The …

FDA Issues Class I Recall After Catheter Sheath Detached Inside Patient During Coronary Imaging Procedure The U.S. Food and Drug Administration (FDA) …

Hundreds of Siemens MRI Machines Recalled After Reports of Pressure Build-Up and Potentially Fatal Helium Leaks During Quench Events The U.S. Food …

FDA Delays Could Put Lives at Risk The safety of medical devices in the United States depends heavily on the timely actions …

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, …