FDA Issues Most Serious Type of Recall for Philips Respironics BiPAP Ventilators — Lives at Risk Without Urgent Action The U.S. Food and Drug Administration...
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 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...
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 In December, the U.S. Food and Drug Administration (FDA) approved a first-of-its-kind artificial blood vessel—Symvess—created by Humacyte...
The recent recall of the Tack Endovascular System by Philips has raised concerns about the safety of medical devices used in critical procedures. The recall...
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...
Exciting BioZorb news, KBA assumes leadership role in BioZorb lawsuits concerning the BioZorb recall. KBD Partner Robert Price Appointed to BioZorb Leadership Team to Take...
CereLink Intracranial Pressure Monitor Recall – A Critical Medical Device Failure The CereLink Intracranial Pressure (ICP) Monitor, designed to measure brain pressure in critically ill...
