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A new class action lawsuit against Whirlpool Corporation addresses refrigerators alleged to have defective wiring that compromises the appliance’s functionality and safety.

If you bought a Whirlpool refrigerator, you likely did because the company has an outstanding reputation of making quality products. But, according to the plaintiffs, the wires, designed to flex with the opening and closing of the refrigerator doors, are prone to fraying or breaking prematurely due to the use of substandard materials.

This defect, often manifesting within a few years of purchase, significantly hinders the refrigerator’s performance by disabling critical features such as ice makers and water dispensers—key selling points emphasized in Whirlpool’s marketing materials. Furthermore, the plaintiffs highlight an alarming safety concern: the risk of electrocution or fire stemming from exposed, live wires, a danger exacerbated by the presence of water and known to refrigerator manufacturers like Whirlpool.

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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.

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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.

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Online vape retailers, manufacturers, and labeling laboratories are at the center of a proposed class action lawsuit, which claims that consumers were misled into purchasing vape pens containing levels of hemp-derived delta-9 tetrahydrocannabinol (delta-9 THC) that exceed the legal threshold.

The lawsuit, initiated by lead plaintiff Hannah Ledbetter, asserts that she bought delta-8 vape pens from Cloud 9 Online Smoke & Vape LLC under the impression that the product labels accurately represented their contents. This case was brought forth on Tuesday to the US District Court for the Northern District of Georgia.

According to the legal filing, Ledbetter had the purchased vape pens subjected to laboratory analysis, which purportedly revealed that the actual THC content far exceeded the amounts stated on their labels, showing a delta-9 THC concentration higher than the legally allowed limit of 0.3 percent on a dry weight basis.

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The answer to this question varies depending on the specific class action settlement. Carefully review the claim filing instructions to determine whether proof of purchase is necessary when submitting your claim form.

Certain class action settlements specifically require certain forms of proof from claimants, such as a store receipt, product packaging, or another court-approved document, to support your claim for an award. However, many other settlements do not require proof of purchase for participation.

In some settlements, you may have the option to choose whether to include proof of purchase with your claim form. Typically, class members who furnish proof of purchase are eligible for a higher payout compared to those who do not provide evidence of their product or service acquisition.

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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

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On this page, our lawyers will explain exactly who is eligible to file a Roundup cancer lawsuit. Will summarize the basic eligibility criteria that our firm is currently using to screen potential Roundup cases; and we will discuss the relevant injuries involved in the Roundup lawsuits.

About the Roundup Lawsuits

For decades, Roundup was the leading brand of herbicide (weed killer) on the market. Roundup was originally developed and manufactured by Monsanto, until 2017 when Monsanto was bought out by Bayer.

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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.

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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.

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Our legal team is actively involved in Suboxone litigation, specifically focusing on lawsuits related to tooth decay. Our attorneys are representing individuals affected by tooth decay, broken teeth, and other dental injuries caused by Suboxone.

Suboxone lawsuits are being pursued because the defendants were aware of the drug’s propensity to cause severe dental issues, yet failed to inform the public.

While a warning was eventually added in 2022, these Suboxone lawsuits seek justice for individuals who suffered dental injuries prior to this warning. These victims, unaware of the risks associated with Suboxone, experienced tooth decay and other dental problems without sufficient warning or justification.