FDA Issues Early Alert on Automated Impella Controller Fixation Issue: What Patients and Hospitals Need to Know The U.S. Food and Drug Administration (FDA) has...
Philips Respironics DreamStation Ventilator Recall: Dangerous Programming Errors Put Patients at Risk The U.S. Food and Drug Administration (FDA) has issued another urgent warning involving...
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...
Medtronic's Left Heart Vent Catheter Recall: A Wake-Up Call for Medical Device Quality At Ketterer, Browne & Davani (KBD) Attorneys, we closely track issues involving...
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™...
