Articles Posted in Mass Torts

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For many years, courts across the country have been flooded with hernia mesh lawsuits. These product liability claims allege that certain permanent hernia mesh implants were defectively designed, inadequately tested, poorly labeled, or sold without proper warnings about the risk of serious complications after surgery.

The lawsuits involve several major medical device manufacturers, including Ethicon, C.R. Bard and Davol, Covidien, and Atrium Medical Corp. The cases are not true class actions. They are mostly individual personal injury lawsuits consolidated into separate federal multidistrict litigations, or MDLs, based on the manufacturer and product involved.

The hernia mesh litigation looks very different in 2026 than it did five years ago. Some defendants have resolved most of their claims. Bard has moved into settlement administration after a major global settlement framework, although claims are still being filed against Bard.

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From the early 1950s to the late 1980s, the Marine Corps base at Camp Lejeune in North Carolina provided residents and employees with drinking water heavily contaminated with toxic chemicals.

Extensive scientific research has revealed that the poisoned water supply at Camp Lejeune had a devastating impact on the long-term health of base residents, who have suffered significantly higher rates of birth defects, cancer, and neurological conditions.

Our lawyers are not taking new clients in this litigation. This page provides the latest updates on the Camp Lejeune litigation and addresses some of your key questions as this litigation drags on.

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In the world of antibiotics, Bactrim (sulfamethoxazole-trimethoprim) stands as a powerful weapon against bacterial infections. It works great. This combination medication, composed of two active ingredients, has saved countless lives by combating a wide range of bacterial invaders.

However, beneath its lifesaving capabilities, Bactrim hides a potential complication – its role in contributing to yeast infections. In this comprehensive article, we delve into the mechanisms of Bactrim, the enigma of yeast infections (Candidiasis), and how the two intersect, shedding light on an often-overlooked aspect of antibiotic treatment.

Bactrim

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Internal bra mesh lawsuits are being filed by women who say surgical mesh used in breast augmentation, breast lift, breast reduction, revision, or post-mastectomy reconstruction caused serious injuries instead of support. Our lawyers are handling these claims.

These cases involve products such as GalaFLEX, GalaFLEX Lite, GalaFLEX 3D, GalaFLEX 3DR, Phasix Mesh, Phasix ST Mesh, and other synthetic or biologic mesh products used to reinforce breast tissue or support implants. The core claims are that the mesh caused infection, chronic pain, nerve damage, seroma, inflammation, capsular contracture, mesh exposure, implant malposition, reconstruction failure, disfigurement, revision surgery, or removal surgery.

An internal bra is a surgical technique. The mesh is placed inside the breast to provide support beneath the tissue or implant. When it works, the goal is lift, support, and stability. When it fails, the patient can be left with pain, infection, hardening, scarring, deformity, implant loss, or a surgery that has to be redone.

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Spinal cord stimulator lawsuits are being filed by patients who say their implanted pain device caused new injuries instead of relief. Our lawyers are handling these claims.

These cases involve devices made by Boston Scientific, Abbott, Medtronic, Nevro, and other neuromodulation companies. The core claims are that the device migrated, malfunctioned, shocked the patient, burned, failed to control pain, caused neurological problems, required revision surgery, or had to be removed entirely.

A spinal cord stimulator is a surgically implanted device near the spinal cord. The leads sit in the epidural space, and the implanted pulse generator sends electrical stimulation intended to interfere with pain signals. When the device works, it helps patients with chronic pain. When it fails, the patient is often left with worse pain, additional surgery, nerve injury, infection, paralysis, or permanent limitations that did not exist before the implant.

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Grok sexual deepfake lawsuits are being filed against xAI over claims that Grok and related image-generation tools were used to create and spread nonconsensual sexual images of real people. The lawsuits focus on a simple question with serious consequences: Did XAI release and promote a tool that could turn ordinary photos of women, girls, and other real people into sexualized deepfakes without meaningful safeguards?

These are not ordinary internet defamation cases. A sexual deepfake can look real, spread fast, attach itself to a victim’s name, and keep resurfacing after the original post is removed. Survivors describe fear, humiliation, anxiety, depression, loss of privacy, reputational harm, school disruption, work disruption, and the awful feeling that strangers may have saved, shared, or traded fake intimate images of them.

The strongest Grok deepfake cases will be built on proof: the prompt history, the source photo, the generated image or link, the account that posted it, takedown requests, platform responses, police reports, school reports, therapy records, witness statements, and evidence that xAI knew this kind of misuse was foreseeable before more people were harmed.

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Millions of women use chemical hair relaxers regularly. New scientific research three years ago revealed that chronic exposure to the chemicals in hair relaxer products can cause uterine and ovarian cancer. This new evidence prompted a wave of lawsuits against the manufacturers of hair relaxer products by women claiming that they developed cancer as a result of using these products.

These cases are moving forward. The MDL judge has scheduled the first bellwether trial for early 2027.  These trials are intended to help both sides gauge how juries might respond to the evidence and could influence settlement discussions…if there is not a global settlement before the first trial, as many, including our lawyers, suspect.

If you are looking for the most recent updates on hair relaxer lawsuits in 2025, we continue to provide timely information on case progress, bellwether trials, and potential compensation payouts for hair relaxer lawsuits. Our team remains committed to keeping victims informed as this litigation unfolds.

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Numerous women have brought lawsuits concerning vaginal mesh against multiple medical device firms due to injuries stemming from flawed transvaginal mesh implants.

This article aims to outline the issues linked with vaginal mesh implants and their role in precipitating one of the most substantial mass litigation cases in history.

Additionally, it will provide updates on the ongoing vaginal mesh class action lawsuit and answer your questions about potential eligibility for individuals considering initiating their own legal action concerning vaginal mesh complications and what that will entail.

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If your premature baby died or suffered serious injuries from necrotizing enterocolitis (NEC) after being fed with formula such as Enfamil or Similac, you may be able to file a product liability lawsuit and get financial compensation.

Infant formula made from cow milk has been linked to NEC, and there is evidence that the formula companies knew about this link but negligently failed to warn consumers and doctors about it.

About Necrotizing Enterocolitis (NEC)

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If you or a loved one experienced pain, discomfort, or complications after receiving a BioZorb implant following breast cancer surgery, you are not alone. Across the United States, patients are taking legal action to hold the manufacturer, Hologic, accountable for the harm caused by this device.

The BioZorb implant, manufactured by Hologic, Inc., is a class II medical device first cleared by the FDA in 2012 under the 510(k) process. It is an implantable radiographic marker composed of a bioabsorbable material (polylactic acid) and six titanium radiopaque clips, which are designed to mark soft tissue sites during radiation therapy following breast cancer surgery. The device is intended to provide a three-dimensional marker for more precise radiation targeting while gradually dissolving in the body over time.

BioZorb works. But it has also been linked to several complications, including prolonged pain, discomfort, infection, device migration, and non-absorption. Many patients have reported the formation of hardened masses, scar tissue, and additional injuries at the implant site. The device has also been associated with increased radiation exposure and adverse reactions requiring further surgeries for removal.

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