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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 …

FDA Class I Recalls Issued for Impella RP Devices After Sensor Malfunctions Lead to Injuries FDA Finalizes Three Class I Recalls for …

Patients and Families Explore Legal Options Following Boston Scientific AXIOS Stent and Electrocautery-Enhanced Delivery System Recall The U.S. Food and Drug Administration …

FDA Announces Class I Recall of Ivenix Large Volume Pumps After Software Malfunctions Cause Serious Injuries The U.S. Food and Drug Administration …

FDA flags potential high-risk issue after Trividia Health reports injuries and updates safety instructions for millions of glucose monitoring devices Continuous blood …

Millions of recalled FreeStyle Libre devices may be linked to dangerous misreadings, fires, and fatal events. Continuous glucose monitoring (CGM) systems have …

Understanding the FDA’s Warning Letter to Abbott, What It Means for FreeStyle Libre Users, and How Injured Patients Can File Lawsuits On …

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