Olympus Scope Infection Lawsuit

Close-up of an Olympus TJF-Q190V duodenoscope elevator mechanism and a medical illustration of CRE "superbug" bacteria.

Olympus Duodenoscope Infections: October 2025 Safety Alert & Lawsuit Update A critical October 2025 safety notice has linked Olympus TJF-series duodenoscopes to ongoing “superbug” outbreaks and sepsis. Despite following sterilization protocols, patients are contracting drug-resistant infections due to a design defect in the device’s elevator mechanism. If you underwent an ERCP procedure and suffered a severe infection or organ failure, you may be eligible for the 2026 wave of litigation.

Spinal Cord Stimulator Lawsuit

Medical illustration of a spinal cord stimulator lead implanted in the epidural space, highlighting potential areas of nerve damage.

Spinal Cord Stimulators promised chronic pain relief but have left thousands with permanent injuries, including loss of bowel control and paralysis. If you required revision surgery for a device from Medtronic, Abbott, or Boston Scientific, you may be entitled to a settlement. Discover your legal options and get a free case review today.

Cartiva Toe Implant Lawsuit

Close-up of a Cartiva synthetic cartilage toe implant next to a medical diagram of a foot joint.

Stay updated on the Cartiva Toe Implant lawsuit as the JPML moves to consolidate cases in 2026. With failure rates reported as high as 64% and a 2024 FDA recall in place, patients suffering from implant subsidence or seeking revision surgery may be eligible for compensation. Learn about the current case status and your legal rights.

AngioDynamics Port Catheter Lawsuit

Medical port catheter assembly and tubing on a surgical drape, representing the devices involved in the AngioDynamics SmartPort, Vortex, and Xcela lawsuits.

AngioDynamics Port Catheter Litigation (MDL 3125) Lawsuits filed nationwide allege that AngioDynamics port catheters—specifically the SmartPort, Vortex, and Xcela models—suffer from a critical design defect involving barium sulfate. This defect allegedly causes the catheter material to degrade, fracture, or migrate, leading to severe complications such as sepsis, blood clots, and organ perforation. Federal cases have been consolidated into Multidistrict Litigation (MDL No. 3125) in the Southern District of California.

BioZorb Breast Marker Lawsuit Filings

BioZorb breast marker device lawsuit for complications, pain, and infection after breast surgery

Stay up to date on the BioZorb Breast Marker Lawsuit and pending MDL proceedings. This page provides official court filings, Pretrial Orders (PTOs), and Case Management Orders (CMOs) related to claims that the BioZorb surgical marker caused chronic pain, infections, and disfigurement after breast surgery. Check back regularly for updates as the BioZorb lawsuits progress toward federal consolidation and coordinated discovery.

Gore-Tex Hernia Mesh Lawsuit

Gore-Tex hernia mesh device linked to severe complications and lawsuits

Gore-Tex DualMesh was marketed as a breakthrough in hernia repair, but patients have reported severe complications including chronic pain, infections, bowel obstruction, and mesh migration. Made from ePTFE (Teflon), the mesh’s shrinking and porosity can cause long-term injuries requiring surgical removal. Despite these risks, the FDA has not recalled Gore-Tex DualMesh. Attorney Brett Vaughn is currently one of the few lawyers nationwide pursuing cases for those harmed by this device.

Bard Hernia Mesh Lawsuit

Lawsuits on Bard Hernia Mesh

Bard hernia mesh lawsuits are pending in Rhode Island state court and in federal court. Thousands of Bard hernia mesh lawsuits have been filed.

Covidien Hernia Mesh Lawsuit

Lawsuit Over Covidien Hernia Mesh

Covidien Hernia Mesh Lawsuits Covidien is the second largest hernia mesh manufacturer in the world after Bard. In 2014, Covidien was acquired by Medtronic for $42.9 billion. Covidien is located in Massachusetts and Medtronic is located in Minnesota. Like most hernia mesh manufacturers in the United States, Covidien sells polypropylene-based hernia meshes. However, Covidien is […]

BioZorb Breast Marker Lawsuit

Biozorb Marker Lawsuit

BioZorb Lawsuit At Nigh Goldenberg Raso & Vaughn, we are committed to representing individuals who have been affected by the BioZorb implantable radiographic marker device. The BioZorb has been the subject of recent FDA safety communications and recalls, and our team is dedicated to helping those who have suffered adverse effects due to the use […]

Exactech Hip Knee & Ankle Recall Lawsuit

Exactech Lawsuit

Exactech Recall Lawsuit NGRV attorney Ashleigh Raso works extensively on the Exactech hip knee & ankle recall lawsuits. Exactech is a multinational medical device manufacturer that designs and manufactures orthopedic medical devices. Over the last two years, Exactech recalled several thousand hips, knee, and ankle joint replacements.  In the Exactech recall lawsuits, patients allege that […]

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Fill out the form below or call Nigh Goldenberg Raso & Vaughn today for a free consultation 202-792-7927

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Fill out the form below or call Nigh Goldenberg Raso & Vaughn today for a free consultation 202-792-7927

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