United States of America

The Apple AirTag litigation now includes a federal MDL for people who allege that Apple AirTags were used to stalk, track, threaten, or harm them. On October 2, 2026, the Judicial Panel on Multidistrict Litigation consolidated the federal AirTag stalking lawsuits into MDL No. 3199 in the Northern District of California, transferring 17 lawsuits from 13 federal districts to one judge.

There is no AirTag settlement for all victims. Not yet. But Apple says it has already settled a number of individual AirTag stalking claims. The Apple AirTag MDL gives us a chance to screen these cases and put them on an organized path forward. It is rare to be talking settlement this early in an MDL. But Apple has already shown that it is willing to resolve at least some of these claims.

What are these cases about? The core allegation is simple. Apple created a small, inexpensive, remarkably effective tracking device that could be hidden in a car, purse, backpack, or other personal property. For most uses, it is a fantastic device. The problem is Apple knew before AirTag was released that the device could be abused for stalking. Of course, Apple did not want this and built anti-stalking protections. The claim in these lawsuits is that those protections were not nearly enough to protect some victims.

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.

Victims of sexual abuse or assault, either as a child or an adult, have the right to bring a civil lawsuit against both their abuser and any school, company, or organization that might be liable for the abuse.

For decades, schools, churches, and treatment centers have used a playbook to silence victims, destroying records, intimidating survivors, and using legal loopholes to dodge responsibility. But courts are catching up, and new laws in New York are forcing these institutions to pay for the harm they caused.

In this post, we will provide a brief overview of sexual abuse lawsuits in New York. We will explain the applicable statute of limitations for sex abuse civil cases in New York and how settlement amounts are calculated in these cases.

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.

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