Urgent Recall: HeartSine Samaritan Defibrillators

HeartSine Samaritan Defibrillators May Fail When Lives Depend on Them Defective AED devices recalled due to dangerous circuit issue – KBD Attorneys is investigating potential...

Update: BD Alaris™ Infusion Pump Has Legacy Part Failures

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

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...

Latest Abbott HeartMate Recall the Most Serious Yet

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...

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel In December, the U.S. Food and Drug Administration (FDA) approved a first-of-its-kind artificial blood vessel—Symvess—created by Humacyte...

Philips Removes and Discontinues Distribution of Tack Endovascular System

Philips Removes and Discontinues Distribution of Tack Endovascular System Due to User Challenges The recent recall of the Tack Endovascular System by Philips has raised...

Medtronic Recalls Pipeline Vantage Embolization Devices

Medtronic Recalls Pipeline Vantage Embolization Devices Due to Serious Risks Medtronic, one of the largest medical device manufacturers in the world, has issued a recall...

KBA Partner Robert Price Appointed to BioZorb Litigation Leadership Team

Exciting BioZorb news, KBA assumes leadership role in BioZorb lawsuits concerning the BioZorb recall. KBA Partner Robert Price Appointed to BioZorb Leadership Team to Take...

CereLink Intracranial Pressure Monitor Recall

CereLink Intracranial Pressure Monitor Recall – A Critical Medical Device Failure The CereLink Intracranial Pressure (ICP) Monitor, designed to measure brain pressure in critically ill...

FDA Warns of Dangerous Rotarex Atherectomy Device Failures

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...

Defective Medical Devices

Urgent Recall: HeartSine Samaritan Defibrillators

Update: BD Alaris™ Infusion Pump Has Legacy Part Failures

Cook Medical Angiographic Catheter Recall

Latest Abbott HeartMate Recall the Most Serious Yet

FDA’s Controversial Approval of Humacyte’s Artificial Blood Vessel

Philips Removes and Discontinues Distribution of Tack Endovascular System

Medtronic Recalls Pipeline Vantage Embolization Devices

KBA Partner Robert Price Appointed to BioZorb Litigation Leadership Team

CereLink Intracranial Pressure Monitor Recall

FDA Warns of Dangerous Rotarex Atherectomy Device Failures

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