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The Lenovo class action lawsuit alleges that Lenovo sold Flex 5 and Yoga 730 laptops with a defect in the display that significantly impairs the laptops’ functionality.

Despite sending his Flex 5 laptop to Lenovo for repairs twice during the warranty period, the plaintiff, along with many other purchasers, found that the display issues persisted after the repairs. Lenovo was accused of suggesting ineffective repair methods or failing to address the core issue causing the defect.

The lawsuit claims Lenovo knew about this defect but continued to market and sell these laptops, highlighting their high-resolution displays and versatile screen positions as major selling points.

This page will explain what the vaginal mesh or pelvic mesh lawsuits are about and who qualifies to file a vaginal mesh lawsuit. We will discuss the eligibility criteria that our lawyers use to screen these cases and we will look at the primary injuries involve in the litigation.

About the Vaginal Mesh Lawsuits

Vaginal mesh, (also referred to as transvaginal mesh or pelvic mesh), is a specialized surgical mesh implant designed to reinforce and strengthen weakened or damaged tissue during surgical procedures, particularly in female pelvic reconstructive surgeries. These surgeries are used to treat conditions like pelvic organ prolapse and stress urinary incontinence, which stem from weakened pelvic muscles causing organs like the uterus, bladder, or rectum to descend into the vaginal area. The goal of surgical intervention with vaginal mesh is to repair and bolster these weakened muscles.

Millions of women use chemical hair relaxers on a regular basis. In 2022, new scientific research 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.

Our mass tort lawyers have been at the forefront of the hair relaxer cancer lawsuits from the very beginning. We are currently accepting hair relaxer cancer cases from women across the country.

About Hair Relaxers

TRESemmé is a popular brand of shampoo and other hair care products made by Unilever, Inc. Recently, consumers have filed lawsuits alleging that TRESemmé shampoo contains harmful chemicals such as formaldehyde that have caused users to suffer hair loss.

About Unilever and TRESemmé

Unilever is a major manufacturer of personal care products and it is the second leading manufacturer of shampoo in the world. TRESemmé is one of Unilever’s most popular hair care brands. The TRESemmé Products are sold directly by Unilever through retailers.  Unilever promotes TRESemmé Products through labeling and advertising channels, including representations written or approved by Unilever on retail websites like Walmart.

On this page we will explain who is eligible to file an Exactech implant recall lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential Exactech lawsuits; and we will describe the relevant injuries being alleged in the Exactech cases.

What Are the Exactech Recall Lawsuits About?

Exactech is a medical device company that specializes in making surgical implant systems for use in joint replacement surgeries such as knee, hip and ankle replacements. In August 2021, Exactech annouced a massive recall covering all of its knee and ankle replacement implants manufactured in 2004 or later.

On this page we will look at who qualifies to file a Truvada lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential Truvada lawsuits; and we will describe the relevant injuries being alleged in the Truvada cases.

What Are the Truvada Lawsuits About?

Truvada is a prescription drug used for the treatment and prevention of HIV. It helps to control the HIV virus and prevent it from being transmitted to partners. The active ingredient in Truvada is tenofovir disoproxil fumarate or “TDF” which was developed by Truvada’s manufacturer, Gilead Pharmaceuticals.

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.

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.

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).