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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.

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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.

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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).

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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.

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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.

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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.

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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.

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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.

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For several years, courts across the nation have been inundated with thousands of pending hernia mesh lawsuits. These product liability claims assert that hernia mesh implants from various manufacturers were defective, causing diverse complications post-surgery.

The lawsuits encompass multiple hernia mesh products produced by four medical device companies: Ethicon (a subsidiary of Johnson & Johnson that has recently settled most of its lawsuits), C.R. Bard (now part of Beckton Dickinson), Covidien, and Atrium Medical Corp. Lawsuits against each defendant have been consolidated into distinct class action MDLs.

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We can all agree that NFL apparel is expensive.  A new lawsuit against the NFL claims that antitrust violations are a big part of the reason.

A class action lawsuit has been filed against the National Football League (NFL) and sports merchandise leader Fanatics in a Manhattan federal court. An Illinois resident accuses the NFL and its 32 teams of conspiring with Fanatics, based in Jacksonville, Florida, to monopolize the online retail market for licensed sports merchandise like jerseys and t-shirts. The suit claims this has led to consumers paying artificially high prices due to stifled competition.

The lawsuit alleges that instead of engaging in competitive sales, the NFL and its teams have effectively given Fanatics exclusive control over the market, with the sports merchandise company sharing its monopoly profits with the teams. This arrangement is said to have disadvantaged other retailers.

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