United States of America

Our lawyers are reviewing hair relaxer cancer lawsuits for women across the United States. These claims involve women who used chemical hair relaxers or hair straighteners for years and were later diagnosed with uterine cancer, including endometrial cancer, ovarian cancer, or serious uterine fibroids that led to a hysterectomy.

The federal hair relaxer litigation included 12,381 pending lawsuits as of October 1, 2026. The cases are moving through expert discovery and bellwether preparation in the Northern District of Illinois. This litigation has been going on for years, but there is still no global hair relaxer settlement or MDL payout program.  That does not mean our lawyers are not bullish on these cases. We are. It is just moving slowly, which is how it goes sometimes in the MDL mass torts. We still expect a favorable global settlement when all is said and done.

The strongest cases generally involve frequent, long-term use followed by uterine or ovarian cancer, a clear product history, and substantial treatment or reproductive injury.

Bard PowerPort lawsuits allege that defects in implanted port catheters can cause fractures, migration, blood clots, infections, embolisms, and other serious complications. Thousands of product liability lawsuits are now pending against Bard and its parent company, Becton Dickinson, in a federal multidistrict litigation in Arizona. After a long slog, these cases are now moving forward.

The first bellwether trial ended with a partial defense verdict and a deadlocked jury on the central design defect claim. The most recent completed trial, Divelbliss v. C.R. Bard, led to a $40 million verdict. It involved an alleged fracture of a silicone Groshong catheter. Five bellwether trials are now expected to run through February 2027. The first two trials produced very different results, and the third trial began in October 2026. Our lawyers remain bullish on well-documented fracture, migration, and embolization cases.

This page provides the latest Bard PowerPort lawsuit updates, projected settlement amounts, and information about who may qualify to file a claim.

Massage therapy is meant to offer healing, comfort, and stress relief, not fear or trauma. But in recent years, a disturbing number of sexual assault lawsuits against massage therapists have been filed across the United States. Women and men alike have come forward to report abuse during massage sessions at both independent practices and national spa franchises, including Massage Envy, MassageLuXe, Hand & Stone, Elements Massage, Spavia, and Woodhouse Spa.  Our lawyers handle these cases nationally.

Many of these cases raise the same ugly question. Did the spa know, or should it have known, that the therapist presented a danger to customers? Lawsuits allege failures in hiring practices, background checks, supervision, and the handling of prior complaints. Some of the most troubling cases involve therapists who allegedly continued working after someone had already reported misconduct.

At the heart of these claims is the violation of a deeply personal boundary. Victims often report feeling trapped, exposed, and powerless, assaulted under the guise of treatment. And when spas fail to take swift action or try to silence or dismiss complaints, the trauma deepens.

Our lawyers are now focusing our attention on the Medtronic Bravo CF capsule recall.

This device is used to diagnose acid reflux and gastroesophageal reflux disease (GERD). In September 2026, the FDA classified a major recall of these devices as Class I, the agency’s most serious recall category.

This should be a simple no-frills test. A doctor attaches a small capsule to the lining of the patient’s esophagus. The capsule measures acidity and transmits readings to a receiver the patient wears. The goal is to determine whether the patient has acid reflux.

This page is about social media addiction lawsuits and who is eligible to bring a claim. Our lawyers also provide the latest news on social media lawsuits, including the upcoming trial in California and the federal social media addiction MDL.

The problem that led to social media lawsuits is that millions of people, too many of whom are children, are addicted to social media platforms such as Facebook, Instagram, Snapchat, TikTok, and YouTube. For these vulnerable users, social media addiction can be very harmful and lead to things like eating disorders, depression, self-harm, and, in some cases, suicide.

Now, these companies are facing a wave of lawsuits alleging that they knowingly designed the algorithms of their platforms to lure young people into harmful addictions.

Thousands of hernia mesh lawsuits are pending in courts across the country. Our hernia mesh lawyers are handling these cases in all 50 states.

The plaintiffs in these lawsuits are individuals with defective hernia mesh implanted during surgery, causing them to suffer severe post-surgical complications and injuries.

The hernia mesh lawsuits involve multiple hernia mesh products made by four medical device companies that are in (or were in) the litigation: Ethicon (a Johnson & Johnson subsidiary that has reached a settlement in most of its lawsuits), C.R. Bard (now part of Becton Dickinson), Covidien, and Atrium Medical Corp.

This page explains the Suboxone tooth decay lawsuits, the dental injuries linked to Suboxone film, and where the federal MDL stands in 2026.

The core claim in the Suboxone litigation is straightforward: plaintiffs allege that Indivior and related defendants knew, or should have known, that Suboxone film could cause severe dental damage, including tooth decay, enamel erosion, broken teeth, tooth loss, and expensive dental reconstruction. Plaintiffs contend the companies failed to warn patients and prescribing doctors until the FDA required a dental warning in 2022.

Our lawyers are still taking selected Suboxone tooth decay lawsuits in 2026. We are screening these cases more carefully than we did earlier in the litigation. We know more now and, from seeing literally thousands of cases, we have a tighter handle on what we think will generate a Suboxone settlement.

Chlorpyrifos lawsuits allege that repeated exposure to this widely used insecticide can contribute to Parkinson’s disease. The people most likely to bring these claims are farmers, pesticide applicators, pest control workers, groundskeepers, greenhouse employees, and others who personally mixed, loaded, sprayed, or cleaned up chlorpyrifos products over months or years.

Chlorpyrifos (CPF) was sold under trade names that include Dursban, Lorsban, Cobalt, Nufos, Bolton, Stallion, Pilot, Warhawk, and Hatchet. It was used on farms, golf courses, ornamental plants, and residential and commercial properties. Many workers remember the trade name but not the active ingredient. Product identification is therefore one of the first and most important parts of investigating a claim.

Quick answers

Uber is defending thousands of sexual assault lawsuits brought by passengers who say they were sexually assaulted by Uber drivers. Plaintiffs are asking what Uber knew about the risk of sexual assault, how it screened drivers, what happened when complaints came in, and whether the company could have done more to keep dangerous drivers off the platform. In the $8.5 million verdict, jurors confirmed what we have been saying all along.

Federal cases have been consolidated in In re: Uber Technologies Inc., Passenger Sexual Assault Litigation, MDL No. 3084, in the Northern District of California. In an MDL, each survivor still has her own lawsuit and her own damages.

By October 2026, 4,916 cases were pending in the federal MDL, with additional claims proceeding in California state court. A federal bellwether case scheduled for October was settled before opening statements. We expect another trial to be scheduled soon.

A spinal cord stimulator is an implantable medical device used to manage chronic pain, most often involving the back or spine. These systems are marketed as a way to reduce pain by interrupting nerve signals before they reach the brain. But for a growing number of patients, the device fails to help. It introduces new and sometimes permanent problems, including electrical shocks, burning pain, infections, lead migration, hardware failure, and repeat surgeries to reposition or remove equipment that was supposed to improve quality of life.

This page explains spinal cord stimulator lawsuits and why they are being filed nationwide. It focuses on what patients are alleging, how these devices have failed in real-world use, and why many of these cases go beyond ordinary medical malpractice claims. The most serious lawsuits do not center on a single surgical mistake. They examine how modern spinal cord stimulators were designed, tested, and approved, and whether patients were ever adequately warned about the risks that now recur repeatedly in medical records and FDA reports.

Many victims want to know what spinal cord stimulator settlement amounts will look like and how we think compensation will be calculated, assuming an ultimate settlement. Settlement amounts and payouts in these cases will depend on several factors, which we dig into more fully below.

Contact Information