FDA Issues Class I Recall of Abiomed’s Impella Controller Due to Cybersecurity Risk A Digital Threat With Real-World Consequences for Heart Patients The U.S. Food...
Olympus Issues Voluntary Recall for ViziShot 2 FLEX Needles: What Patients & Providers Should Know On September 19, 2025, Olympus Corporation announced a global voluntary...
FDA Finds Safety Risks in Boston Scientific Heart Devices When medical devices designed to save lives instead put patients at risk, the consequences can be...
Abiomed’s Impella Recall and the Future of Cardiovascular Device Innovation When the U.S. Food and Drug Administration (FDA) issues a Class I recall, it signals...
Update: BD Alaris™ Infusion Pump Recall Expands Due to Legacy Part Failures KBD Attorneys Continues to Investigate Defective Medical Device Injuries Linked to BD’s Alaris™...
Cook Medical Angiographic Catheter Recall At KBD Attorneys, we regularly investigate product recalls involving medical devices, especially when those products place patients at risk of...
Medtronic Recalls Life-Support Ventilators After Serious Injuries and a Death In June 2025, Medtronic issued a Class I recall—the most serious type—on its Newport HT70...
FDA Deems Latest Abbott HeartMate Recall the Most Serious Yet In another alarming development for patients relying on mechanical heart support, the FDA has classified...
Philips Allura and Azurion Patient Table Recall Medical device recalls are always concerning, especially when they involve equipment used in critical healthcare settings like operating...
FDA Warns of Dangerous Rotarex Atherectomy Device Failures: The U.S. Food and Drug Administration (FDA) has issued a warning regarding serious safety concerns with rotarex...
