DuraGen Dural Graft Recall; Integra LifeSciences Boston

DuraGen Dural Graft Recall; Integra LifeSciences Boston DuraGen, a dural graft matrix manufactured by Integra LifeSciences Boston, is widely used in neurosurgery to protect the...

Impella RP Recall

The Impella RP Recall: Updates to the Use Instructions for Impella RP with SmartAssist and Flex We are litigating Impella recall cases, and there are...

FDA Inspection of the Impella Connect

Our law firm is handling Impella heart pump matters. The Impella Connect is one such matter. Abiomed is the manufacturer of the the Impella 2.5,...

BioZorb Lawsuit – Important Victory for Patients in BioZorb Marker Lawsuit

We provide updates concerning the BioZorb lawsuit. The BioZorb marker is no longer on the market. We continue updating the public about the BioZorb lawsuits...

Philips Cardiac Telemetry Recall: Updated FDA Classification

Philips Cardiac Telemetry Recall: Updated FDA Classification and What It Means for Patients The FDA escalated its recall classification for Philips’ outpatient cardiac telemetry system...

BioZorb Recall – FDA’s Warning Letter to Hologic, Inc.

BioZorb Recall - FDA Warning Letter to Hologic, Inc.: What It Reveals About the BioZorb Marker Update concerning the BioZorb recall. On December 18, 2024,...

HeartMate II Recall and Heartmate 3 Recall – Heartmate Injury and Heartmate Death

Approaching the One-Year Anniversary of Abbott’s HeartMate II and Heartmate 3 Recalls Abbott makes a medical device called the Heartmate. The FDA approved the Heartmate...

Boston Scientific Recall – Accolade Pacemaker Recall

As part of our continuing effort to fight for patients injured by defective heart devices, we posted information about the Boston Scientific recall, specifically the...

Impella Heart Pump Recall – Perforated Left Ventricular Wall

Understanding the Dangers of a Perforated Left Ventricular Wall: Implications for Patients Affected by the Impella Heart Pump Recall When surgeons use a medical device...

The Cartiva Implant Saga is Coming to an End – The Cartiva Toe Implant Recall

The Cartiva implant is a medical device a company. Cartiva sold a toe implant in the United States from about 2016 to 2024. After lawsuits...

Defective Medical Devices

DuraGen Dural Graft Recall; Integra LifeSciences Boston

Impella RP Recall

FDA Inspection of the Impella Connect

BioZorb Lawsuit – Important Victory for Patients in BioZorb Marker Lawsuit

Philips Cardiac Telemetry Recall: Updated FDA Classification

BioZorb Recall – FDA’s Warning Letter to Hologic, Inc.

HeartMate II Recall and Heartmate 3 Recall – Heartmate Injury and Heartmate Death

Boston Scientific Recall – Accolade Pacemaker Recall

Impella Heart Pump Recall – Perforated Left Ventricular Wall

The Cartiva Implant Saga is Coming to an End – The Cartiva Toe Implant Recall

KBA Office Locations

Maryland

North Carolina

Florida

Massachusetts