Articles Posted in Mass Torts

Video game addiction lawsuits seek to hold gaming companies accountable for exploiting vulnerable players, particularly minors and young adults, through intentionally addictive game designs.

Gaming addiction has caused significant harm, including mental health struggles, social isolation, sleep disruption, academic decline, financial strain, and family conflict. The lawsuits allege that gaming companies prioritized profit over user safety by designing games to keep children and young adults playing longer, spending more money, and returning even when the games were harming them.

Our attorneys examine claims involving Fortnite, Roblox, Minecraft, Call of Duty, Grand Theft Auto, Apex Legends, Madden, FIFA, and other online games. Below, we look at who may qualify, the video game addiction settlement value our lawyers project for successful claims, and the latest developments in court.

Our lawyers are handling baby powder lawsuits in all 50 states in 2026. The talcum powder lawsuits against Johnson & Johnson have been ongoing for years. The lawsuits allege that prolonged use of talcum powder (or “talc”), the active ingredient in products such as Baby Powder and Shower to Shower, can cause ovarian cancer in some women.

This page provides an update on J&J talc powder litigation and discusses the settlement amounts in ovarian cancer lawsuits for victims.

Latest News on J&J Talc Powder Lawsuit Update 2026

Gabapentin lawsuits are now being filed over dementia, mild cognitive impairment, memory loss, and other serious cognitive problems. New research has raised concerns about a link between these injuries and long-term or repeated gabapentin use.

These cases are still developing, and we are in the early rounds of this. The deeper our lawyers dig into these cases, the more we believe in them.

Now, the litigation is starting to move forward. It seems the center of the litigation will be in state court in Philadelphia. A mass tort program for lawsuits involving gabapentin, sold as Neurontin, and pregabalin, sold as Lyrica, has been established there.

Our law firm is handling baby food autism lawsuits in all 50 states.

Several popular brands of baby food contain high levels of heavy metals such as mercury, arsenic, lead, and cadmium. These heavy metals are well-known neurotoxins. Thousands of children may have developed autism and other neurodevelopmental disorders due to toxic metals found in baby foods.

A growing number of parents are pursuing a toxic baby food lawsuit to hold manufacturers accountable for their children’s exposure to harmful contaminants. These baby food autism lawsuits allege the manufacturers knew about heavy metals in their products, and children developed autism from consuming them. 

Our lawyers stopped accepting new Tylenol autism and ADHD cases after Judge Denise Cote excluded the plaintiffs’ causation experts, a ruling that led to the dismissal of the federal lawsuits.

There is now real reason for renewed optimism. In July 2026, the Second Circuit overturned the judgments resulting from Judge Cote’s expert testimony rulings. The defendants then asked the appeals court to reconsider, and, as we discuss below, that request has now been denied.

But our firm has not yet resumed accepting new Tylenol autism or ADHD claims. The appeals court did not decide that Tylenol causes autism or ADHD, and important questions about the expert evidence still have to be addressed on remand. We will continue following the litigation and reassess our position as the next steps become clearer.

Between 2013 and 2024, contaminated Olympus duodenoscopes infected hundreds of patients at hospitals across the United States. At least 35 people died from these medical scopes.

What happened?  These awful infections were caused by dangerous, drug-resistant bacteria that were extremely difficult to treat.

So you had patients who went to the hospital, often getting diagnostic or therapeutic procedures that they did not think would be a big deal, only to come out with infections that damaged organs, required months of intensive care, or, tragically, proved fatal.

Dupixent lawsuits are now moving forward in federal court for patients who allege the drug caused, accelerated, or unmasked cutaneous T-cell lymphoma and related T-cell lymphomas.

On June 4, 2026, the Judicial Panel on Multidistrict Litigation centralized the federal Dupixent cases in MDL No. 3180, In re: Dupixent (Dupilumab) Products Liability Litigation, in the District of New Jersey before Judge Zahid N. Quraishi.

Dupixent, also known as dupilumab, is a biologic medication used to treat atopic dermatitis, asthma, COPD, and a host of other inflammatory conditions. For many patients, Dupixent has provided real relief where other treatments failed. But for some patients, the story has been very different and not one they could have expected.

Our lawyers handle Paraquat lawsuits in all 50 states. This page provides the latest news and updates on Paraquat lawsuits in both state and federal courts. We also give our perspective on where this litigation is heading and provide projected settlement payouts for a viable Paraquat lawsuit.

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Breast mesh lawsuits allege that some manufacturers promoted or allowed their mesh products to become widely used in breast reconstruction, augmentation, and revision procedures despite the fact that FDA has not cleared or approved any surgical mesh product for use in breast surgery. The FDA has specifically stated that the safety and effectiveness of surgical mesh in breast surgery, including augmentation and reconstruction, has not been determined.

These internal bra lawsuits allege that manufacturers of products such as AlloDerm, GalaFLEX, Phasix, AlloMax, FlexHD, Strattice, and DuroSorb marketed their devices for breast reconstruction, augmentation, and revision surgeries even though those breast-specific applications had not been adequately studied or cleared by the FDA. Patients were not warned. Surgeons were not given enough information. So when complications developed, including infection, mesh failure, chronic pain, implant loss, breast deformity, and the need for additional surgery, many women had no reason to connect their injuries to the mesh product placed inside them.

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