Published on:

By

In 2021, the cellular wireless network company T-Mobile experienced a major “data breach” that caused the personal information of millions of their customers to be exposed to potential hackers. A class action lawsuit was filed against T-Mobile on behalf of all wireless customers who had their information exposed. That lawsuit eventually resulted in a $350 million settlement available to all impacted customers. On this page, we will explain the story behind the T-Mobile customer data breach lawsuit and outline the details of the settlement.

Following a cyberattack in 2021 that exposed the personal information of millions of customers, T-Mobile reached a settlement of $350 million to address allegations of negligence leading to the breach. This settlement marked the second-largest in U.S. history for a data breach, with Equifax’s $700 million settlement in 2019 being the largest.

The deadline for submitting claims to be part of the substantial payout was Monday, January 23, 2023. However, shortly before this deadline, on January 19, 2023, T-Mobile disclosed another cyberattack that affected a minimum of 37 million current customers.

Continue Reading
Published on:

By

On this page, we will look at who qualifies to file a talcum powder lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential talc lawsuits; and we will describe the relevant injuries associated with these cases.

About the Talcum Powder Lawsuits

Talcum powder is a mineral-based powder made from talc, a naturally occurring mineral. Talc is composed of magnesium, silicon, and oxygen. The powder has a soft, silky texture and is widely used in various cosmetic and personal care products. Talc is a common ingredient in cosmetic products such as baby powder, body powders, and face powders. It is used for its ability to absorb moisture and provide a smooth texture.

Continue Reading
Published on:

By

On this page we will look at who qualifies to file a Bard PowerPort port catheter lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential PowerPort lawsuits; and we will describe the relevant injuries associated with the PowerPort lawsuits.

About the Bard Port Catheter Lawsuits

The Bard PowerPort, manufactured and designed by Bard Access Systems, Inc. (now a subsidiary of Becton, Dickinson and Company), is a fully implantable vascular access catheter system. This system is created to facilitate repeated access to the vascular system for administering medications, intravenous fluids, nutrition solutions, and blood products, commonly employed in chemotherapy for cancer patients.

Continue Reading
Published on:

By

On this page, we will look at who qualifies to file a hernia mesh lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential hernia mesh lawsuits; and we will describe the relevant injuries associated with the hernia mesh lawsuits.

What are the Hernia Mesh Lawsuits About?

A hernia mesh is a small net or mesh used by doctors during hernia surgeries to strengthen and support the muscle tissue wall. Due to the frequency of hernia surgeries, thousands of these mesh implants are employed every year. Lawsuits primarily focus on permanent hernia mesh implants, distinct from dissolvable mesh. Permanent mesh is designed to remain in the body indefinitely after implantation, unlike dissolvable mesh. Unfortunately, some permanent hernia mesh implants exhibited design flaws, leading to severe complications after implantation.

Continue Reading
Published on:

By

Truvada is a prescription drug used for the treatment and prevention of HIV. Truvada and similar HIV drugs have been around since the early 2000s, but recent scientific research has shown that long-term use of Truvada can cause serious kidney problems and loss of bone density. Individuals who used Truvada for HIV treatment and subsequently suffered kidney damage, bone weakness, or other injuries are now filing Truvada lawsuits and seeking financial compensation. Our Truvada lawyers are actively seeking new cases from qualified plaintiffs across the U.S.

About Truvada

Truvada is manufactured by the California biopharma company Gilead Sciences Inc. Truvada was first released in the U.S. in 2002 at which time it was one of the very first of a new generation of drugs used to treat and prevent the spread of Human Immunodeficiency Virus (HIV).

Continue Reading
Published on:

By

On this page, we will explain who might be eligible to file an Ozempic lawsuit. Our Ozempic lawyers will explain what qualifying criteria our firm is using to screen Ozempic injury cases and we will also discuss what the primary injuries are in the Ozempic lawsuits.

What Are the Ozempic Lawsuits About?

Ozempic is a prescription medication used to treat type 2 diabetes. Its active ingredient is semaglutide, which belongs to a class of drugs called glucagon-like peptide-1 (GLP-1) receptor agonists. Ozempic is administered by injection and works by mimicking the effects of a natural hormone in the body that helps regulate blood sugar levels.

Continue Reading
Published on:

By

On this page, we will explain who might be eligible to file a toxic baby autism lawsuit. We will explain what qualifying criteria our firm is using to screen baby food autism cases and we will also discuss what the potential settlement value of these cases might be.

About the Baby Food Lawsuits

The lawsuits alleging that toxic heavy metals in popular baby food products caused children to develop autism, originated out of an investigation report from a Congressional Subcommittee entitled Baby Foods are Tainted with Dangerous Levels of Arsenic, Lead, Cadmium, and Mercury (the “Congressional Report”). The Congressional Report publicly revealed that many of the most popular brands of baby food products were tested and found to contain very high levels of various heavy metals known to be toxic to humans.

Continue Reading
Published on:

By

On this page we will explain who might be eligible to file an AFFF firefighting foam cancer lawsuit. We will explain what qualifying criteria our firm is using to screen AFFF cases and we will also discuss what the primary injuries are in the AFFF cases.

About the AFFF Firefighting Foam Lawsuits

AFFF stands for Aqueous Film-Forming Foam. It is a type of firefighting foam that is used to suppress flammable liquid fires, particularly those involving hydrocarbons. AFFF contains water, fluorochemical surfactants, and other additives. The foam works by forming a thin film on the surface of the flammable liquid, creating a barrier that separates the fuel from the air and suppresses the release of flammable vapors.

Continue Reading
Published on:

By

On this page, our product liability lawyers explain who is potentially eligible to file a Paraquat lawsuit based on the current criteria that our firm is using to screen potential Paraquat cases. We will also discuss the potential settlement value of Paraquat lawsuits and what information Paraquat plaintiffs must provide in the class action MDL.

About the Paraquat Lawsuits

Paraquat is very strong industrial herbicide that is used in commercial farming across the U.S. Paraquat is actually illegal in most countries, but in the U.S. licensed farmers can buy it. Paraquat is manufactured by Syngenta, a global agro chemical company headquartered in Switzerland. In the U.S., Paraquat is usually sold under the brand name Gramoxone.

Continue Reading
Published on:

By

On this page, we will look at who qualifies to file a Suboxone tooth decay lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential Suboxone lawsuits, and we will describe the relevant injuries associated with the Suboxone lawsuits.

About the Suboxone Lawsuits

Suboxone is a prescription drug that is commonly used for the treatment of opioid addiction recovery. There is overwhelming evidence showing that Suboxone causes chronic dry mouth which can lead to acute tooth decay and tooth loss. The manufacturers of Suboxone were aware of this side effect for more than a decade but failed to include any warning about tooth decay on the drug product label.

Continue Reading