Category: Medical Devices

Transvaginal Mesh

Pelvic Mesh Victim Awarded $41 Million in Philadelphia Lawsuit Against J&J Ethicon

Johnson & Johnson’s Ethicon unit has been slammed with a $41 million penalty in a lawsuit filed by a woman who claimed severe complications from the company’s pelvic mesh.

Knee Implant X-Ray

Knee Replacement Revision Surgery Lawsuit

Our lawyers are filing lawsuits for knee replacement patients who required revision surgery within 3 years of their initial surgery due to failed bone cement or implant devices.

Doctor Holding MRI Scan

Visualase Recall Lawsuit

The Medtronic Visualase MRI-Guided Laser Ablation System was recalled in September 2018 amid concerns the device’s laser can overheat during use, resulting in severe brain damage, tissue damage, and other serious injuries to the patient.

Essure

Essure Study Receives New FDA Protocol

The U.S. Food & Drug Administration (FDA) on Thursday issued an update on new steps to revise Bayer’s post-marketing study of its Essure birth control device, to ensure that accurate long-term safety data is collected following removal of the IUD...

NeuroBlate-System

NeuroBlate Lawsuit

The NeuroBlate System, a brain surgery probe that utilizes laser therapy to remove cancerous tumors, was recalled in March 2018 after being linked to multiple reports of brain damage -- including at least one which resulted in death -- suffered...

Alcon Cypass Micro Stent

Alcon CyPass Micro-Stent Recall Class Action

Our class action lawyers are filing lawsuits for people who suffered eye damage after undergoing cataract surgery with the Alcon CyPass Micro-Stent.

Alcon Cypass Micro Stent

Alcon CyPass Recall Lawsuit

The Switzerland-based medical company Alcon has announced an immediate withdrawal of the CyPass Micro-Stent from the global market after a study linked the device to an increased risk for severe, potentially irreversible eye damage and other serious side effects.

Distressed Woman

Votiva Lawsuit

‘Vaginal rejuvenation’ procedures, including the Votiva FormaV and FractoraV treatments made by InMode Aesthetic Solutions, have not been approved for use by the FDA, and could be dangerous to women’s health.

Distressed Woman

Vaginal Rejuvenation Class Action Lawsuit

Medical laser devices marketed for a procedure called “vaginal rejuvenation" to women for stress urinary incontinence (SUI) or sexual / menopausal symptoms have not been adequately studied and are linked to adverse health consequences including vaginal burns and scarring, the...

Distressed Woman

Vaginal Rejuvenation Lawsuit

The U.S. Food and Drug Administration (FDA) has contacted several companies that manufacture laser devices, requesting that they stop marketing them for a procedure known as “vaginal rejuvenation,” claiming they are dangerous and could increase the risk of significant health...