Class Actions - Lynch Law Firm

Class Actions

In 2021, Neutrogena and Aveeno recalled some aerosol sunscreen products after discovering they contained benzene. This is an industrial chemical that has been linked to various cancers, like leukemia and non-Hodgkin’s lymphoma.

Anyone who used these recalled products and was later diagnosed with cancer may be eligible to file a sunscreen recall lawsuit. Lynch Law Firm, PC is currently investigating these types of lawsuits, so if you think you may have a valid case, call our defective product lawyers today to find out if we can help you.

Our firm represents defective product victims on contingency, which means the initial legal consultation is free of charge and there are no upfront costs if you hire us to represent you. We have obtained millions on behalf of our clients.

Call Lynch Law Firm, PC today to discuss possible legal options: (800)-518-0508.

Which Sunscreens Were Recalled?

In the summer of 2021, results of an independent test of many sunscreen products revealed several aerosol sunscreens contained benzene. These products were subsequently pulled from the market by Johnson & Johnson:

These products were available at numerous retailers across the nation, such as CVS.

While these were the only products that were recalled, the study conducted by Valisure identified many more products that contain benzene, including products from these popular brands:

Some of the products that contained benzene included:

The study identified a total of 14 products from these popular brands that had benzene at levels higher than two parts per million. Another 26 products had benzene at somewhere between two parts per million and 0.1 parts per million. You might think these levels are too low to cause harm, but there is no safe amount of benzene exposure.

How Do I Know if I Can File a Sunscreen Recall Lawsuit?

Have you been diagnosed with one of the following forms of cancer after using one of the aerosol sunscreens that was found to contain benzene?

If the answer is yes, you may be able to file a sunscreen recall lawsuit. Our experienced lawyers can discuss your situation with you in a free legal consultation. We will need to review several factors to determine your eligibility for a lawsuit, including:

If we determine you may have a case, there are no upfront costs to hire a lawyer.

Call Lynch Law Firm, PC today to learn more: (800)-518-0508.

What are the Risks of Benzene Exposure?

Benzene has many uses, as it is used in the manufacture of pesticides, rubber and plastic. However, it is dangerous to human beings, as the International Agency for Research on Cancer lists benzene as a human carcinogen. The Food and Drug Administration (FDA) and the Environmental Protection Agency (EPA) also classify benzene as carcinogenic to people.

The IARC says there is evidence exposure to benzene can cause acute myeloid leukemia. There is also research connecting benzene exposure to acute lymphocytic leukemia, chronic lymphocytic leukemia, multiple myeloma and non-Hodgkin lymphoma.

Research posits that benzene can trigger chronic inflammation, which can suppress the immune system. This may increase the risk of developing cancerous cells.

If you apply sunscreen that contains benzene, your body absorbs it and can send it into your bloodstream.

Potential Symptoms of Leukemia

There are various symptoms that may indicate you are suffering from leukemia, which may have been caused by using sunscreen that contained benzene. These symptoms may include:

You should seek medical care if you begin experiencing these symptoms. While each situation is unique, it is generally true that leukemia and other cancers are easier to treat if you catch them early.

Damages From a Sunscreen Recall Lawsuit

The purpose of a product liability claim is to not only hold the manufacturer liable for putting consumers at risk, but also to provide compensation to victims who suffered damages. These damages may include:

An experienced lawyer can help you gather the evidence you will need to prove the value and existence of your damages. This is particularly important with non-economic damages like pain and suffering. We can help you document the emotional effects of a cancer diagnosis, including the effect on your marital relationship.

Call Lynch Law Firm, PC To Discuss a Sunscreen Recall Lawsuit

People use sunscreen to help prevent overexposure to dangerous UV rays, but some Neutrogena and Aveeno sunscreens may have put people at higher risk for various forms of leukemia.

If you or your loved one were diagnosed with cancer after using one of these recalled products, give us a call to discuss possible legal options. While compensation cannot erase what happened, it can help victims pay for past and ongoing medical care and other damages their diagnosis has caused.

We manage defective product cases, like sunscreen recall lawsuits, at no upfront charge. The initial legal consultation is also free.

Lynch Law Firm, PC. Experienced Lawyers. Proven Results. Phone: (800)-518-0508.

Our firm is currently investigating lawsuits against Invidior PLC, the manufacturer of Suboxone. The drug is meant to help people overcome opioid addiction, but has been linked to tooth decay and other severe dental injuries.

Dozens of people have already filed lawsuits seeking compensation for the cost of dental care and other damages. If you or a loved one have suffered tooth decay, tooth loss or other serious dental injuries, call Lynch Law Firm, PC to discuss a potential Suboxone tooth decay lawsuit.

Our dangerous drug lawyers do not charge upfront fees and the initial legal consultation is free of charge. When pharmaceutical companies distribute unreasonably dangerous products, and they do not adequately warn the public of the risks, they should be held accountable.

Our law firm has obtained millions on behalf of injured victims. Call today: (800)-518-0508.

Who May Be Eligible to File a Suboxone Tooth Decay Lawsuit?

You should review the eligibility criteria with an experienced lawyer. He or she can help you determine if you may have the right to file a lawsuit to seek compensation for your damages.

However, if your situation fits the following criteria, you may be eligible to take legal action:

Your lawyer can help you gather the evidence you will need to support your claim, such as:

What Dental Injuries Could Suboxone Cause?

Suboxone strips have been connected to the following dental injuries, which has led to numerous lawsuits:

These injuries require expensive treatment, such as extracting damaged teeth or the use of implants or dentures. Dentists may recommend fluoride treatment or special toothpaste to help counteract the loss of tooth enamel. You may need to undergo painful operations like root canals or meet with a periodontist to address problems with your gums.

Contact Lynch Law Firm, PC to discuss a possible Suboxone tooth decay lawsuit. Phone: (800)-518-0508.

Compensation for Victims of Suboxone Sublingual Strips

If you suffered any of the injuries listed above after taking Suboxone, you may be able to file a lawsuit to recover compensation, which may include:

Our licensed attorneys are prepared to pursue full compensation for all damages suffered. You should not be burdened with these damages if they were caused by a negligent drug manufacturer.

Why Does Suboxone Damage Patients’ Teeth?

Suboxone (buprenorphine) is prescribed to treat patients who are addicted to oxycodone, morphine, hydrocodone or other opioids. Each dose is a thin strip patients place under their tongue. As the strip dissolves, much like teeth whitening strips, patients feel like they are getting a small dose of an opioid. Over time, this may help them break their addiction to opioids.

The problem with these medicated strips is their acidity. As the strips melt, acid is released into patients’ mouths, which disrupts pH balance. Over time, the acid can wear down teeth and gums, leading to serious injuries. It takes at least 30 minutes for one strip to dissolve in your mouth, meaning your teeth are continuously exposed to acidity as the strip continues to dissolve.

Suboxone can also limit the product of saliva in your motion. Saliva is the body’s defense against acid. This means your teeth and gums become more susceptible to injury as you continue using Suboxone.

Research as far back as 2013 links Suboxone strips to severe dental injuries. Researchers studied patients at Brigham and Women’s Hospital in Boston who were taking buprenorphine to treat their opioid addiction:

A research letter that came out in the Journal of the American Medical Association in late 2022 found that patients taking Suboxone strips had a much higher risk of dental problems.

Another study from 2023 showed that sublingual Suboxone users had a much higher rate of dental disorders compared to those taking the drug in pill form. Researchers analyzed reports of adverse events from the Food and Drug Administration’s Adverse Event Reporting System.

Has the FDA Taken Any Action to Protect the Public?

The FDA has not recalled Suboxone over concerns about dental injuries. However, it did put out a drug safety communication in January 2022. The document caused the manufacturer to add a warning label to Suboxone packaging.

The FDA’s communication warned about the risk of dental injuries after taking buprenorphine in strip form. The FDA said people had reported dental problems like:

The communication advised patients not to discontinue use of the medication, but they should talk to their doctors about the risks. The document also recommended ways to reduce the risk of dental injury, such as swishing water around your mouth after the medication fully dissolves.

This warning from the FDA could be used to support a Suboxone tooth decay lawsuit, as it helps show a connection between dental injuries and use of sublingual Suboxone.

Have There Been Any Settlements or Verdicts in Suboxone Tooth Decay Lawsuits?

We are in the early stages of Suboxone tooth decay litigation, so there have not been any settlements. However, these lawsuits were consolidated into a multidistrict litigation (MDL) in early February 2024. As of April 1, 2024, there were 44 cases in the MDL.

An MDL is a way of speeding up the legal process when there are numerous cases against one defendant involving similar allegations. The Suboxone tooth decay lawsuits claim the manufacturer did not adequately warn people about the risk of serious dental injuries.

For example, a man from Maryland filed a lawsuit after developing severe tooth decay after taking Suboxone to help with opioid addiction. A woman in Georgia filed a lawsuit claiming Suboxone caused resulted in the need for tooth extractions.

If you think you may have a valid Suboxone lawsuit, contact us today to discuss your situation.

Call Lynch Law Firm, PC to Discuss a Suboxone Tooth Decay Lawsuit

Tooth decay and tooth loss are more than physical injuries. They can be psychologically devastating, lowering self-esteem and quality of life.

Dental injuries also add more stress to the lives of those who are trying to recover from opioid addiction.

Suboxone manufacturers should be held liable for the economic and non-economic damages their drugs may have caused. They are legally obligated to avoid putting dangerous products on the market and properly warning patients and doctors of the risks.

Contact us today to find out if you may be eligible to file a Suboxone tooth decay lawsuit. An initial consultation with an experienced attorney is free and there are no upfront costs if you hire our firm.

Contact Lynch Law Firm, PC today to discuss legal options. Phone: (800)-518-0508.

Lawsuits are being filed across the country and against the makers of Ozempic for injuries, most notably gastroparesis, which have been linked to the use of this popular drug.

At Lynch Law Firm, PC, we believe drug makers, manufacturers and retailers of dangerous drugs should be held accountable for injuries and damages their drugs cause. If you or a loved one took Ozempic and are now suffering from gastroparesis, we may be able to help. Contact our law offices to discuss your situation, including whether you may have legal options.

Worried about the cost? We take injury lawsuits on contingency. This means no cost and no risk to you.

Not sure if you have a case? Our firm can help you with that as well. We charge you nothing up front, and we only get paid for our services if we win your case.

Call Lynch Law Firm, PC to learn how we may be able to help you. Phone: (800)-518-0508.

What Is Ozempic and How Could It Be Causing You Harm?

Ozempic is a medication that has been widely advertised as a leading treatment for helping to improve blood sugar levels in adults who have type 2 diabetes. It has also become extremely popular for helping patients to lose weight.

Unfortunately, continued use of Ozempic is causing hundreds of patients to suffer severe gastrointestinal issues. Common complaints about the drug include:

Why Are the Ozempic Lawsuits About?

Patients are suing Novo Nordisk, the Danish drug company that manufacturers Ozempic. The primary claim is that Novo failed to warn consumers or their doctors about certain serious complications of taking Ozempic. Gastroparesis is one of the most common complications of patients taking Ozempic.

What Is Gastroparesis?

Gastroparesis is a serious medical condition where the stomach muscles do not work properly. Food takes much longer than normal to process.

This delayed or reduced functioning of the stomach is a chronic condition that does not go away on its own.

According to the UCLA School of medicine, there are three stages of gastroparesis:

How Do I Know If I Am Eligible To File a Lawsuit Against Ozempic?

If you were prescribed Ozempic to treat diabetes or manage your weight loss, you may be eligible. Other factors that need to be considered for eligibility include the following:

While there is no real cure for this condition, symptoms can be managed.

There are multiple treatments and therapies that can help patients to manage the systems. Depending on what stage of gastroparesis a patient has, more intensive treatment may be required.

Treatments may include:

How Much Could an Ozempic Lawsuit Be Worth?

It is not possible to determine the value of an Ozempic lawsuit without considering multiple unique factors of each case.

Generally speaking, if taking Ozempic led to severe medical complications, such as gastroparesis or even tooth loss, you may be eligible to recover compensation for certain damages, such as:

How Can an Attorney Help Me With an Ozempic Lawsuit?

A lawyer who has a history of proven results in cases involving dangerous drugs could greatly benefit your claim. These cases are often long and complicated. You want someone on your side who has extensive knowledge of the law and who is prepared to work diligently on your behalf.

Have Questions After Taking Prescription Ozempic? Call Lynch Law Firm, PC Today

If you or a loved one suffered severe medical complications after taking Ozempic, we urge you to contact our law offices in New Jersey as soon as possible. You can speak to a licensed attorney at our firm to get answers to your legal questions and to find out if you may have a valid claim.

Lawsuits for dangerous drugs, like Ozempic, have deadlines, and robust cases take time to build. The longer you wait to call a lawyer, the harder it will be for him or her to build a solid case.

We fight to get you the results you need. Contact Lynch Law Firm, PC: (800)-518-0508.

Multiple scientific studies suggest that Tylenol taken during pregnancy may be linked to an increased risk of a baby having autism.

Did you take Tylenol or a generic form of acetaminophen (also known as paracetamol) during pregnancy? Has your child also been diagnosed with autism, ADHD or a neurodevelopmental disorder? If so, you may be eligible to seek compensation in a lawsuit against the manufacturers and retailers of Tylenol.

Contact Lynch Law Firm, PC to learn more about this lawsuit. A licensed attorney at our firm is prepared to discuss the details of your unique situation and determine whether you may have legal options. There is no cost or risk for this initial consultation, and you do not have to come to our office in person.

It is important to note that deadlines apply, so you should call our law offices as soon as possible.

Request your FREE case review today. (800) 518-0508

What Are The Tylenol Autism Lawsuits About?

As a result of extensive scientific research, mounting evidence has linked the frequent use of acetaminophen during pregnancy to a higher risk of a child being diagnosed with autism.

The class action lawsuit, which is being handled as a multidistrict litigation, or MDL, alleges that Tylenol, its manufacturers and retailers breached its state-law duty of care by failing to warn about the link between frequent acetaminophen use during pregnancy and autism.

Defendants named in the lawsuits are not limited to, but include:

Parents of children with autism allege that Tylenol should have provided a warning and details of these studies. Having this knowledge before using this product would have given parents the power to make an informed decision for their unborn children during pregnancy.

What Is Multidistrict Litigation?

Multidistrict litigation (MDL) is a legal procedure used in the United States federal court system to streamline the handling of complex civil cases involving multiple plaintiffs and defendants. In an MDL, similar lawsuits filed in different federal districts are transferred to a single federal district court for pretrial proceedings. This consolidation aims to avoid duplicative discovery, prevent inconsistent rulings, and conserve judicial resources.

While the cases of an MDL are centralized for pretrial purposes, they remain distinct and may return to their original districts for trial if a settlement is not reached. MDLs are commonly used in cases involving product liability, mass torts, and other complex litigation where numerous plaintiffs allege similar injuries or damages against one or more defendants.

Scientific Evidence Linking Prenatal Tylenol Use to Autism and ADHD

The Nature Reviews Endocrinology medical journal published a Consensus Statement back in September 2021 on the use of Tylenol during pregnancy. The statement, issued by a group of 91 leading medical experts, followed significant scientific evidence and warned consumers about the potential link between acetaminophen, also called paracetamol, and autism.

Other studies linking prenatal Tylenol use to autism and ADHD include:

Who May Have a Valid Tylenol Autism Case?

If you took Tylenol during your pregnancy and your child was diagnosed with autism on the spectrum, you may be eligible to file a lawsuit against the manufacturers and retailers of Tylenol. However, you cannot just say you took some form of acetaminophen during pregnancy, you must be able to provide some evidence.

To determine if you may have a case, you will need to discuss the details of your situation with an experienced attorney. This case review is completely free and can be done in person or over the phone.

To help establish evidence of prenatal Tylenol use, we may ask these and other questions:

How Much Compensation Could a Tylenol Autism Lawsuit Be Worth?

Estimations are difficult to make in advance of any lawsuit, especially given there may be other contributing factors that could have an impact on the outcome of a case.

If eligible, compensation could be significant. Compensation awarded could help with the ongoing costs related to your child’s medical costs and other treatments or therapy related to your child’s autism diagnosis.

What Are the Most Recent Updates Related to the Tylenol Class Action Lawsuit?

As of April 2024, the Tylenol autism MDL includes 524 cases for plaintiffs claiming for autism and ADHD cases. As of the same date, another MDL for Acetaminophen had over 600 plaintiffs.

Health professionals maintain their stance on the use of Tylenol or its generic forms during pregnancy.

In December 2023, Denise Cote, the MDL judge in the case, rejected all five of the plaintiff’s expert witnesses. Despite this legal blow to the case, Judge Cote is allowing a new opportunity in the Tylenol MDL case.

On March 18, 2024, Judge Cota will allow a new expert, Dr. Roberta Ness, to introduce new expert testimony. Defendants in the case have until July 2024 to object to this expert’s testimony.

Contact Lynch Law Firm, PC To Discuss Your Eligibility

At Lynch Law Firm, PC, we have been representing injured victims and their families for decades.

Big brands, like Tylenol, as well as their manufacturers and retailers, have a legal duty to warn consumers about potential side effects or harm that could result from using their product.

Our experienced dangerous drug attorneys are dedicated to protecting your rights and recovering the maximum possible compensation on your behalf.

Request your free case review today. There is no risk and no obligation to file a claim. If you have a case and you choose our firm to represent you, there is nothing to pay up front. We only get paid if you do.

Experienced Lawyers. Proven Result. (800) 518-0508

Doctors have used surgical mesh tens of thousands of times to treat hernias. The mesh is meant to promote healing and prevent hernias from coming back.

Unfortunately, thousands of people have suffered severe complications from hernia mesh, such as organ damage, infections, device migration and bowel obstruction.

If you or a loved one suffered serious injuries or complications from hernia mesh or needed revision surgery, our defective medical device lawyers may be able to help you. We are investigating hernia mesh lawsuits against Atrium, Covidien and Ethicon, companies that are facing thousands of legal claims from victims. This litigation is ongoing and cases continue to be added.

Contact Lynch Law Firm, PC today to learn more about these cases and whether you may able to join the ongoing hernia mesh litigation. Your initial legal consultation is free, and there are no upfront costs to engage our services.

Call today to discuss your injuries and potential legal options. Phone: (800)-518-0508.

Injuries and Complications From Defective Hernia Mesh

Hernia mesh is designed to support damaged, weak tissue around hernias. The problem is hernia mesh products have been linked to many severe injuries and complications, which are often treated with revision surgery. Some of the complications and issues include:

These complications can cause prolonged pain and victims often need revision surgery. Additional surgery prolongs your recovery and puts you at risk for further complications.

If you or a loved one has dealt with any of the complications listed above, call Lynch Law Firm, PC to discuss potential legal options. We can discuss a hernia mesh lawsuit against Ethicon, Covidien or Atrium. We are also investigating C.R. Bard hernia mesh lawsuits.

Who Can File a Hernia Mesh Lawsuit?

Anyone who experienced the injuries or complications detailed above from Atrium, Ethicon Physiomesh or Covidien hernia mesh, may have the right to file a lawsuit. Generally, you must have experienced these complications from a hernia surgery that occurred on January 1, 2006, or later.

However, you need to review your situation with a licensed attorney in a free legal consultation. A lawyer must determine if your claim is still allowed by the relevant statute of limitations. Once the statute of limitations passes, you lose the right to seek compensation.

Sometimes one law firm says a victim does not have a case while another determines the victim has a valid claim.

There are numerous factors to consider about your eligibility for a hernia mesh lawsuit, so you should call Lynch Law Firm, PC right away to discuss your situation.

Call today to set up your free legal consultation. Phone: (800)-518-0508.

What Damages Can I Include in a Lawsuit?

Victims of a defective hernia mesh may be able to pursue compensation for various damages, including:

If you have questions about the value of a hernia mesh lawsuit, or the merits of your claim, call Lynch Law Firm, PC. Medical device manufacturers that produce defective products should be held accountable for the damages they cause.

Have Any Manufacturers Recalled Hernia Mesh?

Yes, manufacturers have taken various hernia mesh products off the market. If doctors implanted any of these recalled products and you were injured by them, call Lynch Law Firm, PC to discuss a hernia mesh lawsuit.

Atrium C-QUR Recall

In August 2013, the Food and Drug Administration (FDA) recalled tens of thousands of the following Atrium C-QUR hernia mesh patches:

The recall was issued because of problems with packaging. These issues damaged the Omega-3 coating, making the mesh more likely to fail and cause complications and injuries.

Ethicon Physiomesh

Between 2005 and 2014, Ethicon recalled 18,000 Proceed hernia mesh units. The recall notice said the packaging could cause the mesh to lose its coating, creating a higher risk of bowel fistulas and adhesions.

Ethicon also recalled its Physiomesh Flexible Composite mesh in Australia and Europe in 2016. Technically, these products were not recalled in the U.S. The company did a market withdrawal, sending out a safety notice telling doctors to stop using Physiomesh in laparoscopic surgery. The notice said the rate of hernia recurrence and revision surgery was higher than other similar hernia meshes. This data was from large independent registries in Denmark and Germany.

Covidien

Back in October 2018, Covidien issued a recall of more than 7,000 units of the Parietex Composite Parastomal Mesh because of device failure. Patients experienced more hernias, pain and bulging.

Did you suffer injuries or complications from any of these hernia mesh products? Call Lynch Law Firm, PC to discuss a potential hernia mesh lawsuit.

Ongoing Hernia Mesh Litigation

There are four hernia mesh multidistrict litigations (MDL) including tens of thousands of cases. A multidistrict litigation combines similar cases into one legal action in one court. MDLs are meant to help speed up the legal process, especially discovery.

As of April 1, 2024, these are the numbers of pending legal actions in each MDL:

There have been several bellwether trials in these MDLs. A bellwether trial can be thought of as a test trial, although the results are legally binding. These trials help to give both sides a better idea about how juries are likely to rule in future cases involving the defective product.

Bellwether trials in the Covidien MDL could take place in early 2025.

What Do These Lawsuits Allege?

While there are thousands of cases, they all make similar allegations. The plaintiffs claim the hernia mesh products made by these companies are more likely to break down and injure patients, such as by moving or adhering to organs or tissue.

Plaintiffs also allege the manufacturers failed to properly warn patients and doctors about the risks. This exposed patients to an unreasonable risk of serious injuries.

Have There Been Any Notable Settlements?

There have been several settlements of hernia mesh lawsuits, including:

Contact Lynch Law Firm, PC To Discuss a Hernia Mesh Lawsuit

If you have suffered complications from hernia mesh, you might feel overwhelmed by the idea of a hernia mesh lawsuit. That is why you need to discuss your situation with an experienced lawyer.

Victims of hernia mesh or other defective medical devices do not need to go through the legal process alone. They can be guided by licensed attorneys who manage every step on their behalf, and there are no upfront costs to pay.

If you think you may have a case, contact Lynch Law Firm, PC to discuss your injuries and legal rights.

Free initial legal consultation. Call today: (800)-518-0508.

Roundup, one of the most commonly used weed killers, has been linked to various forms of cancer in multiple studies. In March 2015, the International Agency for Research on Cancer (IARC) classified glyphosate, the main ingredient in Roundup, as being “probably carcinogenic.”  This revelation put Monsanto, an agricultural product manufacturing giant, under scrutiny for not warning consumers about the cancer risks.

If you have cancer that may be linked to exposure to Roundup, we strongly recommend you seek legal help right away. Deadlines apply, so it is vital you do not delay. We offer a completely free case review, so there is no risk in having a conversation to learn if you have legal options.

At Lynch Lawyers, PC, we have been helping victims injured by the negligence of others for decades. Our firm has a proven track record, and we are prepared to guide you throughout the legal process. There are no upfront costs to pay if we represent you.

Call to request your FREE case review today: (800) 518-0508

What Do I Need To Know About Roundup?

Roundup is a powerful herbicide used to control weeds on over 168 million acres nationwide. This popular weed killer was developed by Monsanto, a trusted and leading brand in agricultural biotech for over a century. There is no dispute about the effectiveness of Roundup as a weed killer. The issue is with glyphosate, the main ingredient in Roundup and also the focus of many studies linking glyphosate to various forms of cancer.

Who Has the Greatest Risk of Developing Cancer From Roundup?

Individuals most at risk for developing cancer from Roundup are those who used the weed killer frequently and over a long period. Certain people may have been exposed to Roundup regularly and over an extended period may include:

What Are the Main Health Risks of Using Roundup?

Significant research that spans decades links glyphosate as a probable cause of cancer. Studies conducted between 2008 and 2015 specifically associated glyphosate with:

In 2015, the International Agency for Research on Cancer (IARC) announced that studies revealed glyphosate was a probable carcinogen to humans. The Agency for Toxic Substances and Disease Registry came out in support of these findings in 2019.

What Symptoms May Accompany Non-Hodgkin’s Lymphoma?

Non-Hodgkin’s lymphoma is so named because it is a type of cancer that begins in your lymphatic system. Your lymphatic system normally helps you fight off sickness and infections. These types of white cells, called lymphocytes, are the infection fighters, and they live in your lymph nodes, spleen and bone marrow. When these white blood cells start growing out of control, it can result in cancerous tumors.

Symptoms of this cancer may include:

If you experience several of these symptoms, it is important you see a doctor immediately. Treatment options for this type of cancer may include a combination of chemotherapy, radiation therapy, immunotherapy and stem cell transplant therapy.

How Do I Know if I Am Eligible To File a Roundup Lawsuit?

Have you used or been exposed to Roundup? Have you been diagnosed with cancer, such as non-Hodgkin’s lymphoma?  If so, we recommend speaking with an experienced attorney to find out whether your medical condition may be linked to using this weed killer. At Lynch Lawyers, PC, our knowledgeable attorneys have extensive experience handling class action lawsuits for injured victims. We are prepared to review your medical history and determine whether exposure to Roundup may be linked to your cancer diagnosis.

Generally, these are some of the factors that may help to determine your eligibility:

When meeting with one of our licensed attorneys, these are some of the questions you may be asked in your free case review. One of our attorneys will also explain what documentation you need to provide to support your potential claim. For instance, receipts can help to show you previously used Roundup. Medical records will support your diagnosis.

How Long Do I Have To File a Roundup Lawsuit?

There is limited time to take legal action. Even if you are unsure about your eligibility, it is not a good idea to wait to contact a lawyer. We offer a completely free case review to discuss your situation and potential legal options. If we believe you may have a case, there are no upfront fees or costs to pay.

How Much Compensation Can I Expect?

Every case is unique, and we cannot guarantee a specific monetary outcome. If you have a valid case, you may be eligible to recover compensation to cover these and other damages:

Past cases against Monsanto have resulted in awards ranging from millions to billions of dollars. However, awards like these cannot be guaranteed and may vary greatly, depending on the specifics of your unique situation.

Need Legal Help for Cancer Related to Roundup? We Are Here To Help.

Navigating any lawsuit while dealing with an injury or illness can be daunting. At Lynch Lawyers, PC, our firm is deeply committed to holding manufacturers accountable for their negligence. If we represent you, we are prepared to manage all aspects of your case. This means gathering the evidence you need to build a robust, ensuring you do not miss any deadlines and handling all the complex aspects of a class action lawsuit.

Our defective product attorneys are experienced and ready to fight tirelessly to recover the maximum possible compensation on your behalf. If you have lost a loved one to illness linked to Roundup, we can also guide you through filing a claim on their behalf.

Call our law offices 24/7 to get started today: (800) 518-0508

Bard PowerPort catheters have been linked to serious injuries, including blood clots, infections and migration of the device inside the body. More than 100 victims have filed lawsuits against the manufacturer seeking compensation for their injuries and damages.

If you think you or your loved one might have a case, call Lynch Law Firm, PC today to discuss your situation. An initial consultation with a licensed defective medical device lawyer is free of charge. There are also no upfront fees if we take your case.

We have a history of obtaining millions for those injured by the negligence of others.

Have legal questions? Call Lynch Law Firm, PC today to discuss a Bard PowerPort lawsuit: (800)-518-0508.

Who May Be Eligible To File a Bard PowerPort Lawsuit?

If you suffered an injury after being implanted with a Bard PowerPort, you may be able to file a lawsuit. However, you need to review the details of your injury and treatment with an experienced lawyer to determine if you have a viable case.

These are some of the types of victims who may be able to pursue legal action:

If you or a loved one fits any of these criteria, call Lynch Law Firm, PC to discuss whether you can file a Bard PowerPort lawsuit.

Evidence for a PowerPort Claim

To be eligible for a Bard PowerPort lawsuit, you will need comprehensive evidence to prove you were injured after being implanted with this device.

Evidence that can help to support your claim includes detailed medical records. These records can establish that you were implanted with a PowerPort catheter and suffered an injury or complication as a result. Just having an injury and suffering complications is not enough, however. You also need to show that you were treated for injuries and complications that are more likely than not linked to the surgically implanted catheter.

Your lawyer may work with you to document the many effects of your injuries. One important way to record your injuries is to document the healing progress, the level of pain and suffering you experience daily and how these injuries are impacting your daily quality of life. You can take pictures of your injuries and add them to this journal as well. Other evidence can include testimony from family and friends. They can help to explain how your complications have affected your life.

Other examples of evidence that may be needed for a lawsuit includes:

Serious Injuries and Complications Caused by Bard PowerPorts

A Bard PowerPort is a device that is made up of two parts: the injection port and polyurethane catheter port.

The injection port is implanted under the skin, either on an arm or in the chest. The port creates an easy access point for injections. The polyurethane catheter port is a flexible tube that is connected to the injection port. The catheter is implanted in one of the central veins that transports blood to your heart.

Unfortunately, the PowerPort is composed of Chronoflex AL, which is a mix of barium sulfate and polyurethane. Chronoflex AL may be the reason catheters can break and migrate to other regions of the body.

Device migration is just one of the many serious injuries and complications that may result after implantation. Some of the other injuries may include:

Some of these injuries and side effects could have a fatal outcome, depending on various factors, such as the patient’s overall health, age and response to treatment.

While the physical harm from the Bard PowerPort can be significant, there is also an emotional component that should not be ignored.

Have Bard PowerPorts Ever Been Recalled by the FDA?

There have not been any recalls of the Bard PowerPort because of complications or device failure. A recall in March 2020 was because of a barb tip, which is the wrong tip for this type of port. The danger it poses is that it could cause the catheter to dislodge from the tunneler.

Unfortunately, the lack of a recall allows this product to remain on the market, potentially causing harm to more patients. At this point, taking legal action may be the only way to raise awareness about the issue and potentially hold the manufacturers accountable.

It is important to note that you can still file a lawsuit without the product having been recalled. If you were injured after implantation, call Lynch Law Firm, PC to discuss possible legal options.

What Is the Value of My Potential Claim?

The value of a Bard PowerPort lawsuit will depend on many factors, such as:

At our firm, we are committed to helping clients secure full compensation. Compensation allows victims to get all the medical treatment they need and prevent the situation from turning into a financial crisis.

What Are the Plaintiffs Alleging in Their PowerPort Lawsuits?

Lawsuits against Bard name several PowerPorts:

Lawsuits over these and other PowerPort models make several allegations against the manufacturer:

Defective Design and Manufacturing

Plaintiffs claim that the Bard PowerPorts were designed in a way that makes them unsafe. The design increases the risk of fracture, migration and malfunction, which could lead to injury. The lawsuits also allege defective manufacturing.

Failure To Warn

Medical device manufacturers have a legal obligation to warn the public about the dangers of their products. If consumers do not receive adequate warning, they do not have the opportunity to make fully informed decisions.

Lawsuits claim Bard had a significant number of adverse event reports, which may indicate they knew about the increased risk of injuries.

Misrepresentation

Plaintiffs accuse Bard of misrepresenting the safety and reliability of the PowerPorts, thereby misleading healthcare professionals and patients.

Have Any Existing Lawsuits Settled?

In August 2023, Bard PowerPort lawsuits were consolidated into a multidistrict litigation (MDL) in the U.S. District Court for the District of Arizona. The goal of consolidating lawsuits in this way is to speed up the legal process, particularly during discovery. As of April 1, 2024, there are 116 cases in the MDL.

There are no bellwether trials as of spring of April 2024. Bellwether trials are the first cases to be tried in an MDL. The outcome of these cases helps to give both sides a better idea of how juries are likely to rule.

At this point, none of the lawsuits have been settled. However, the MDL continues to grow and eventually there will be bellwether trials.

Call Lynch Law Firm, PC To Discuss a Bard PowerPort Lawsuit

At Lynch Law Firm, PC, we understand the profound impact of defective medical devices on patients and their families. We know how vital it is for victims to secure compensation to help them pay for medical treatment and other damages.

If you have suffered complications from a Bard PowerPort catheter, we may be able to assist you. We work on contingency, so there are no upfront fees to find out if you may have a case. There are also no fees while we work on your case.

When you hire a lawyer, he or she can manage every aspect of your case, from filing the lawsuit to negotiating for full compensation.

Call us to schedule your free legal consultation: (800)-518-0508.

Thousands of people have sued C.R. Bard over serious injuries related to hernia mesh implants. Victims allege C.R. Bard hernia mesh is defective and had an unreasonable risk of failure and complications.

If you or a loved one suffered complications from this company’s hernia mesh products, it is important to review your legal options. Our experienced defective medical devices lawyers at Lynch Law Firm, PC offer a free, no-obligation legal consultation. We also charge no upfront fees to represent injured victims.

Our law firm has a proven history of results in injury cases, having recovered hundreds of millions for our clients. We are committed to securing full compensation from product manufacturers that put people at higher risk of injury.

Have questions about a C.R. Bard hernia mesh lawsuit? Call us today: (800)-518-0508.

Am I Eligible To Join the C.R. Bard Hernia Mesh Litigation?

While every claim is different, many people who meet the following criteria may be eligible to file a lawsuit:

If you meet this criteria, you will also need to provide detailed medical evidence of your original hernia surgery and subsequent treatment for complications.

We strongly recommend that you discuss your situation with an experienced lawyer. That is the best way to determine if you may have a viable case. An experienced lawyer can also explain what your case may be worth and the next steps you need to take.

Complications Linked to C.R. Bard Hernia Mesh Products

Thousands of C.R. Bard hernia mesh lawsuits have cited numerous complications, some of which include:

These complications not only lead to mounting medical expenses, but also severe emotional distress and unnecessary physical pain and suffering. The pain can make it harder to work, complete daily tasks at home and put a strain on relationships.

These are just a few reasons why thousands of people who have dealt with serious injuries and complications from C.R. Bard hernia mesh products have filed lawsuits. Product manufacturers should be held accountable when they put patients at a higher risk of injury.

Why Are These Complications Occurring?

The hernia mesh products named in lawsuits are made of polypropylene, which is a composite plastic. However, the manufacturer of this plastic has a Material Safety Data Sheet telling buyers that the plastic should not be permanently implanted in the body.

Polypropylene is likely to erode/degrade soon after implantation. As this plastic erodes, it increases the surface area for bacteria to cling to, which can release toxins into the body. This reaction has been linked to various complications, like:

Another harmful material in these hernia mesh implants is polytetrafluoroethylene (ePTFE). This material was meant to make the mesh more stable. However, the material is too heavy, which can cause it to be absorbed into patients’ bodies and increase the risk of another hernia, mesh failure and adhesion.

What Are the Lawsuits Claiming?

C.R. Bard hernia mesh lawsuits make several allegations about how the company has put consumers at risk. The lawsuits allege that the company’s hernia mesh:

These lawsuits also claim the doctors who implanted the mesh engaged in malpractice.

The purpose of these lawsuits is not just to secure compensation for victims, but also to hold C.R. Bard accountable for putting patients at risk and prioritizing profits over safety. Defective medical device lawsuits may help improve safety standards and protect patients from injuries in the future.

If you think you may have a case, you need experienced legal assistance to optimize your chances of recovering the compensation you need. Defective medical device cases can be daunting, as the defendants in these cases are well funded and prepared to put up a good fight. Your lawyer needs to gather substantial medical evidence and expert testimonies to establish the link between the hernia mesh and your complications.

Contact Lynch Law Firm, PC today to learn more about how we may be able to help you. Phone: (800)-518-0508.

Compensation From a C.R. Bard Hernia Mesh Lawsuit

Victims of C.R. Bard hernia mesh may be able to seek various forms of compensation. For instance, you may need additional compensation for medical care to cover the costs of revision surgery and any ongoing treatment of hernia mesh complications or injuries.

Compensation may also be available for the following damages :

At Lynch Law Firm, PC, our goal is to maximize compensation for injured victims. While compensation does not erase the harm you suffered, it can help victims to move forward after a serious injury.

History of Hernia Mesh Recalls and FDA Warnings

Hundreds of thousands of hernia mesh products were recalled between 2005 and 2019. This includes the Bard Composix Kugel hernia patch, which happened back in 2005. These products contained a memory recoil ring that could break off and perforate patients’ bowels. The recall for this product was a Class 1 recall, which is the most serious type of recall.

Nine years later, in 2014, the Food and Drug Administration (FDA) released a safety communication about complications from hernia mesh. The six complications listed included:

What Is Happening With the C.R. Bard Hernia Mesh Multidistrict Litigation?

As of April 1, 2024, there are 21,673 actions pending in the C.R. Bard, Inc., polypropylene hernia mesh multidistrict litigation. An MDL is a consolidated legal action with similar cases that is meant to help streamline the legal process. This MDL was formed in 2017 in the Southern District of Ohio.

More cases are being added each month, so you may be able to join the MDL to pursue compensation for your damages. However, there is limited time to act, so you need to contact an experienced lawyer to discuss your situation.

Have There Been Any Settlements or Verdicts?

There have been multiple bellwether trials in the hernia mesh MDL. The first resulted in a verdict for the defense. The second resulted in a $250,000 verdict for the plaintiff. The third bellwether trial resulted in a $500,000 verdict for the victim and the fourth may get underway in April of 2024.

Bellwether trials give both parties a better idea of how juries are likely to rule on the shared questions of fact in the thousands of existing cases. These trials may result in a settlement for many of the cases included in the MDL.

Call Lynch Law Firm, PC To Discuss a C.R. Bard Hernia Mesh Lawsuit

If you or your loved one suffered serious injuries, especially injuries that required revision surgery from a C.R. Bard hernia mesh, Lynch Law Firm, PC may be able to help you secure compensation. There is limited time to take legal action, so it is vital that you act quickly.

Call us to schedule a free legal consultation to learn if you may have a case. There are no upfront costs with our services, and we do not get paid unless our clients get paid.

Our attorneys have been recognized by the legal community for securing results for those we represent. For example, partner Jim Lynch is a past president of the New Jersey Association for Justice.

Experienced lawyers. Proven results. Call us today for legal assistance: (800)-518-0508.

Are you an agricultural worker or farmer who’s faced a Parkinson’s Disease diagnosis after exposure to paraquat herbicide? Was one of your family members diagnosed with this disease after working with this dangerous chemical?

Our law firm is here to help you understand your rights and explore compensation options. Numerous studies have established a connection between paraquat and Parkinson’s Disease, leading to thousands of lawsuits against its manufacturer, Syngenta.

With decades of experience in representing injury victims, our firm has successfully recovered millions for our clients. Our defective product lawyers offer a free, no-obligation consultation, working on a contingency basis – meaning we only get paid if you receive compensation for medical care and other damages. Reach out today to learn how we can assist you with the legal process.

Request your FREE case review today. Call (800) 518-0508.

Am I Eligible for Compensation?

There are many questions we need to answer before we can determine if you may have a valid case for compensation. This includes your medical diagnosis, how you were exposed and how long you were exposed.

Paraquat is heavily regulated and can only be used by licensed applicators. That is why paraquat lawsuits are often filed by people who worked in commercial gardening/landscaping, on farms or as groundskeepers. You may have absorbed this substance through your skin, such as through a cut or rash. Paraquat may have also gotten into something you drank or contaminated food that you ate. Some victims inhaled paraquat, which may have damaged their lungs.

Paraquat is known by various brand names, as this substance is an active ingredient in many herbicides, such as:

Paraquat is one of the most frequently used herbicides in the country, as it is sprayed on more than 100 different crops. It is mainly used to control weeds and grass.

If you have questions about possibly pursuing a case, call Lynch Law Firm, PC today. Our goal is to provide you with comprehensive legal support, ensuring that all aspects of your case are carefully considered.

If you believe you have been exposed to paraquat and have been diagnosed with Parkinson’s Disease, we encourage you to contact us for a detailed case evaluation. There are no upfront costs. Call today to find out how we may be able to assist you in seeking justice and compensation.

Call to learn more. Our lawyers are here to help: (800) 518-0508.

Potential Compensation for Paraquat Victims

Paraquat victims may be eligible for various types of compensation, each tailored to the specific circumstances of their case. This can include:

Each case is unique, and the compensation amount depends on factors like illness severity, exposure length and long-term prognosis. The aim is to alleviate the financial burden of treatment and provide support to those affected by this devastating disease. Our attorneys are committed to securing the maximum possible compensation and holding manufacturers accountable for their negligence.

Controversy Around the Use of Paraquat

The controversy surrounding paraquat centers on its global use and the contrasting approaches to its regulation. While about 100 countries have approved its use, over 50, including China, have banned it. Interestingly, China, one of the manufacturers of paraquat, produces it solely for export.

U.S. Regulations

In the United States, the herbicide is not banned, but it is strictly regulated by the Environmental Protection Agency (EPA). Classified as “restricted use,” only commercially licensed applicators are permitted to use paraquat. The EPA has regulations to help prevent exposure to paraquat, such as including additives like dyes and vomit-inducing chemicals.

Increasing Use

Despite acknowledged risks, paraquat usage in the U.S. has increased, especially as weeds and pests develop resistance to other herbicides like Monsanto’s Roundup, which itself has been the subject of lawsuits.

In 2016 alone, approximately seven million pounds of paraquat were applied across nearly 15 million acres in the U.S. The EPA reapproved its use as recently as October 2020, highlighting the ongoing debate over its safety and the role of regulatory bodies in balancing agricultural needs with public health concerns.

These are some of the crops that get sprayed with paraquat:

Link Between Paraquat and Parkinson’s Disease

The connection between paraquat exposure and Parkinson’s Disease has been a focus of scientific research for decades.

Initial Research

The initial link was suspected in the 1980s following a cluster of advanced Parkinson’s cases in California, which were traced back to a substance that is similar in structure to paraquat. This led to further studies in agricultural areas, often showing abnormally high numbers of Parkinson’s cases.

NIH Study

Numerous studies, including significant research by the National Institutes of Health (NIH), have strengthened the argument for a link between paraquat and Parkinson’s. For one study, the NIH evaluated research on tens of thousands of agricultural workers and spouses. One study author concluded that there was persuasive data linking Parkinson’s to paraquat exposure.

Another notable study in 2012 highlighted the heightened risk for individuals with specific genetic variations who are exposed to paraquat.

Research findings indicate that exposure to paraquat, especially during the teenage or young adult years, can significantly increase the risk of developing Parkinson’s Disease.

Calls for Banning Paraquat

The Michael J. Fox Foundation for Parkinson’s Research, along with other leading Parkinson’s research entities, have raised concerns to the EPA about paraquat’s continued use. The United Parkinson’s Advocacy Council asked the EPA to ban the chemical in 2017.

Paraquat Lawsuits You Should Know About

Most of the paraquat lawsuits being filed are included in a multidistrict litigation (MDL) in the Southern District of Illinois, which was created in June 2021. As of January 2, 2024, there were more than 5,000 cases in this legal action.

MDLs are utilized to streamline pretrial proceedings for cases with similar facts, aiming to reduce costs and prevent inconsistent rulings across different districts. In paraquat cases, victims allege Syngenta and Chevron USA knew about the dangers of exposure and failed to provide adequate warning. There are also allegations about concealing the danger from victims and others.

One of the benefits of an MDL is reducing cost and delays that come with pretrial proceedings.

Some of the legal actions in the MDL are selected as bellwether cases. These cases are tried first to give both sides a better idea of how judges and juries are likely to rule on the cases. This could lead to a settlement agreement for a large percentage of the cases in the MDL.

The first bellwether trial was supposed to happen in October 2023 but was delayed until 2024.

There were numerous lawsuits before the MDL was created:

Call Lynch Law Firm, PC To Discuss Legal Options

If you or a loved one has been diagnosed with Parkinson’s Disease after exposure to paraquat, it is crucial to explore your legal options.

At Lynch Law Firm, PC, we are committed to investigating paraquat claims and holding manufacturers accountable for the risks associated with this herbicide. Our team, backed by a history of securing significant compensation for our clients, offers a free, no-risk consultation.

We operate on a contingency fee basis, meaning we only get paid if you receive compensation. Do not hesitate to reach out to us to discuss the potential for a lawsuit and the compensation you may be entitled to.

Call Lynch Law Firm, PC today to schedule your free consultation and take the first step towards seeking justice.

Schedule a free consultation. Call us at (800) 518-0508.

Research has linked Tepezza with permanent hearing loss and tinnitus (ringing in the ears). Dozens of lawsuits have already been filed against Horizon Therapeutics. These lawsuits claim the company knew about the danger but failed to warn patients about these side effects.

If you or a loved one has experienced hearing loss or tinnitus after taking Tepezza for thyroid eye disease, you may be able to join the multidistrict litigation against Horizon.

The experienced dangerous drug lawyers at Lynch Law Firm, PC, know the profound impact hearing issues can have on your life. We are committed to seeking the maximum compensation to help you and your family during this challenging time.

We have decades of experience securing justice and compensation for victims of personal injuries. We offer potential clients a free initial legal consultation and do not charge fees up front. There is no financial risk in calling our firm to learn how we may be able to help.

Do you have questions about a Tepezza hearing loss lawsuit? Call today: (800) 518-0508.

Who May Be Eligible To File a Lawsuit?

Eligibility depends on several factors, including the timing of the hearing issues relative to the treatment, the severity of the symptoms and the absence of other causes for these symptoms. Our legal team is adept at reviewing medical records and histories to determine if Tepezza could be the culprit behind your hearing loss or tinnitus.

Determining your eligibility to file a Tepezza lawsuit is a critical first step towards seeking justice and compensation for your injuries and damages.

Patients who have taken Tepezza (teprotumumab) for thyroid eye disease and suffered hearing loss or tinnitus may qualify to file a lawsuit. That said, there are many factors your lawyer must consider about your eligibility:

Diagnosis of Thyroid Eye Disease and Tepezza Treatment

You must have been diagnosed with thyroid eye disease and received Tepezza treatment. Documentation of your diagnosis and treatment records (number of infusions, etc.) will be essential in establishing the basis for your claim.

Timing and Onset of Hearing Loss or Tinnitus

There should be a clear timeline that connects the onset of hearing loss or tinnitus symptoms to your treatment with Tepezza. Your lawyer needs compelling evidence that your treatment may be responsible for your hearing issues.

Your lawyer will likely want to answer questions like:

Other Potential Causes of Hearing Issues

Your lawyer must also rule out other potential causes of hearing loss or tinnitus, such as age-related hearing loss, exposure to loud noises or preexisting conditions. Medical evaluations and expert testimonies can help isolate Tepezza as the probable cause of your symptoms.

Impact on Quality of Life

This refers to the ways your hearing loss or tinnitus have affected your daily life, ability to work and overall well-being. Evidence of the negative impact on your quality of life can strengthen your case for compensation.

Our experienced legal team reviews clients’ medical histories, treatment records and personal accounts of how the symptoms have affected their lives to determine eligibility.

There is limited time to take legal action, so it is important to act quickly to protect your rights.

Zero upfront costs. Call Lynch Law Firm, PC today: (800) 518-0508.

The Dangers of Tepezza

Tepezza (teprotumumab) is a breakthrough treatment for thyroid eye disease (TED) that was approved by the Food and Drug Administration (FDA) in 2020. Tepezza is currently the only drug on the market for treatment of TED.

However, like all medications, it comes with its own set of risks and side effects:

Hearing Impairment

A significant number of patients have reported partial or complete hearing loss after starting their Tepezza treatment. This can range from mild to severe and may be temporary or permanent.

Approximately 10 percent of patients in the clinical trials reported hearing issues after taking Tepezza. Then, in 2021, the Endocrine Society published a study that found 65 percent of those who took Tepezza developed hearing loss and other hearing problems.

Horizon Therapeutics added a warning to Tepezza labels about hearing impairment. The warning notes that the drug may cause severe hearing impairment. This may include permanent hearing loss. Doctors should evaluate patients’ hearing before, during and after treatment. The benefits of the drug should be weighed against the risks.

Tinnitus

Ringing or buzzing noises in one or both ears, known as tinnitus, has been a common complaint among Tepezza users.

Muscle Spasms and Cramps

Patients have reported experiencing uncomfortable muscle spasms or cramps, which can be both painful and disruptive to daily activities.

Other Reported Side Effects

Tepezza-related hearing loss is permanent for some patients. Those who do not suffer hearing loss may experience tinnitus, which can have a negative effect on quality of life. Chronic tinnitus can hurt an individual’s mental health, social interaction and the ability to work.

If you are dealing with tinnitus or hearing loss from Tepezza, consider consulting an experienced lawyer to review possible legal options.

Defining Thyroid Eye Disease

Thyroid eye disease, also known as Graves’ orbitopathy, is an autoimmune condition that affects the muscles and tissues around the eyes. Symptoms can include eye bulging, double vision and discomfort.

TED is often associated with Graves’ disease, a disorder characterized by an overactive thyroid (hyperthyroidism). TED can also occur in individuals with normal thyroid function or hypothyroidism. The disease manifests when the immune system mistakenly attacks the muscles and tissues around the eyes, leading to inflammation and swelling.

TED symptoms can cause mild discomfort in some patients, while others suffer severe visual impairment. Common symptoms include:

Damages for a Tepezza Hearing Loss Lawsuit

If you took Tepezza and suffered hearing loss or tinnitus, you can seek compensation for the cost of medical treatment, such as the cost of a hearing aid.

Other forms of compensation in a Tepezza lawsuit may include:

The emotional and psychological toll of hearing loss and tinnitus cannot be understated, and our firm is committed to ensuring that these aspects are fully considered in any legal action.

Have Any Tepezza Lawsuits Been Settled?

As of February 2024, there have not been any settlements or verdicts for Tepezza lawsuits. In June 2023, a multidistrict litigation (MDL) was created to consolidate Tepezza lawsuits in the United States District Court for the Northern District of California. As of February 1, 2024, there were 74 actions pending the MDL.

One of the first Tepezza lawsuits was filed in 2022 by a man from Arizona. He was diagnosed with TED and prescribed Tepezza between June and September of 2020. The plaintiff and his doctor say they were not aware of the risks.

His lawsuit says the manufacturer knew of the danger because of many reports from patients, scientific studies and post-market studies done by Horizon Pharmaceuticals. Despite these reports, the lawsuit says the defendant did not warn patients and doctors of the risks.

The lawsuits in the MDL make similar allegations about the dangers of Tepezza and the manufacturer’s failure to warn.

Call Lynch Law Firm, PC To Discuss a Tepezza Hearing Loss Lawsuit

The decision to take legal action is not one to be taken lightly. However, if you have suffered hearing loss or tinnitus after taking Tepezza, pursuing a lawsuit can be a step towards obtaining compensation for your damages. Our legal team is here to guide you through every step of the process, advocating for your rights and best interests.

For more information or to schedule your free consultation, please contact us today. Let Lynch Law Firm, PC be your advocate in this challenging time as you focus on your health and wellbeing.

Proven Results. No Upfront Costs. Call: (800) 518-0508.