Your Fight Deserves the Right Attorney

AFFF Firefighting Foam

AFFF firefighting foam containing per- and polyfluoroalkyl substances (PFAS) has been used since the 1960s at military bases, airports, and fire training facilities across the United States. These "forever chemicals" do not break down in the environment and have contaminated groundwater, soil, and drinking water supplies serving millions of Americans. The C8 Science Panel established "probable links" between PFAS exposure and six diseases including kidney cancer, testicular cancer, and thyroid disease. MDL 2873, consolidated before Judge Richard Gergel in the District of South Carolina, encompasses over 15,216 personal injury claims against manufacturers including 3M, DuPont, Chemours, Tyco Fire Products, and BASF. Water utility settlements exceeding $12.5 billion have been approved, and the personal injury track is advancing toward bellwether trials with Daubert motions and expert depositions underway.

Allergan Breast Implant Lawsuit

Allergan (now owned by AbbVie) manufactured BIOCELL textured breast implants — including the widely used Natrelle 410 — that were found to cause breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), a rare but serious T-cell lymphoma of the immune system. The FDA determined that women with Allergan BIOCELL implants were approximately six times more likely to develop BIA-ALCL than women with implants from other manufacturers. On July 24, 2019, Allergan initiated a worldwide recall of all BIOCELL textured breast implants and tissue expanders. As of June 2023, the FDA had received 1,264 BIA-ALCL reports globally, with 1,079 — representing 85% of all cases — involving Allergan implants. Sixty-three deaths have been reported, with 37 linked to Allergan products. MDL 2921, In re Allergan BIOCELL Textured Breast Implant Products Liability Litigation, is pending before Judge Michael Martinotti in the District of New Jersey with approximately 1,400 cases. The first bellwether trial is scheduled for October 2026. Women who received Allergan BIOCELL textured implants, were diagnosed with BIA-ALCL, or underwent implant removal due to the recall may have viable legal claims.

Asbestos / Mesothelioma

Mesothelioma is a rare and deadly cancer of the lining of the lungs (pleura), abdomen (peritoneum), or heart (pericardium), caused in virtually every case by exposure to asbestos. Asbestos was widely used in construction, shipbuilding, insulation, automotive repair, and industrial applications throughout most of the 20th century. Workers in these industries — as well as their family members who were exposed through contaminated clothing — face a dramatically elevated risk of mesothelioma, asbestos-related lung cancer, and asbestosis decades after their last exposure. The legal landscape for mesothelioma victims is unique: more than 60 major asbestos manufacturers have filed for bankruptcy and established trust funds totaling over $30 billion. Veterans — particularly Navy veterans who worked in engine rooms and shipyards — account for approximately 30% of all mesothelioma diagnoses. Because mesothelioma has a grim prognosis and the legal process moves faster than in typical personal injury cases, acting quickly after diagnosis is essential to ensuring you and your family receive full compensation.

Baby Food Heavy Metals Lawsuit

The baby food heavy metals litigation targets manufacturers who knowingly sold contaminated infant food. A 2021 House subcommittee report revealed internal testing showing arsenic levels up to 180 ppb, lead up to 886 ppb, and significant cadmium and mercury contamination. MDL 3101 in N.D. California consolidates over 3,200 cases as of early 2026.

Bard PowerPort Catheter

The Bard PowerPort is an implantable venous access device — a small port placed under the skin, typically in the chest — that allows medical professionals to administer chemotherapy, draw blood, and deliver medications without repeated needle sticks. Millions of patients have received PowerPort devices since C.R. Bard introduced them in the 1990s. The devices are especially common among cancer patients who require long-term intravenous access. Beginning in the early 2010s, patients, physicians, and researchers began documenting a disturbing pattern: the polyurethane catheter tubing attached to the port was fracturing inside the body. Fragments of the catheter — sometimes several centimeters long — were entering the bloodstream and migrating toward the heart and lungs. The resulting complications range from serious to fatal: cardiac perforation, cardiac tamponade, pulmonary embolism, sepsis, and endocarditis. Becton Dickinson (BD) acquired C.R. Bard in 2017 for $24 billion, inheriting both the PowerPort product line and the mounting litigation. In 2022, a federal multidistrict litigation was established in the U.S. District Court for the District of Arizona to consolidate cases nationwide. Legal claims proceed under theories of design defect, manufacturing defect, failure to warn, and negligence. Patients who received a PowerPort catheter and subsequently experienced catheter fracture, fragment migration, infection, cardiac complications, or unexplained symptoms may be entitled to substantial compensation.

Birth Injury

A birth injury is harm caused to an infant during labor, delivery, or the immediate newborn period as the result of medical negligence. Approximately 1 in 143 babies born in the United States experiences a birth injury. When a physician, midwife, hospital, or NICU staff member fails to meet the standard of care — by misreading fetal monitoring strips, delaying an emergency cesarean section, failing to initiate HIE cooling therapy within six hours of birth, or improperly using delivery instruments — the consequences can include cerebral palsy, Erb's palsy, hypoxic-ischemic encephalopathy (HIE), and permanent disability requiring a lifetime of specialized care. The average settlement for a catastrophic birth injury is $1 million or more; complex cases involving lifetime care for severe cerebral palsy or HIE can reach $10 million or beyond. Families should act promptly: while infancy tolling rules exist in many states, statutes of limitations vary significantly, and evidence — including fetal monitoring strips, hospital records, and APGAR score documentation — must be preserved.

CPAP Cancer

The 2021 Philips CPAP recall — one of the largest in medical device history — exposed millions of users to carcinogenic foam particles and VOCs. Cancers linked to exposure include nasopharyngeal, lung, kidney, liver, and bladder cancer. MDL 3014 in Pittsburgh is advancing toward bellwether trials in 2026.

Camp Lejeune Water Contamination

Camp Lejeune is one of the largest environmental contamination disasters in American military history. For over three decades, servicemembers, their families, and base workers drank, cooked with, and bathed in water laced with industrial solvents at concentrations hundreds of times above safe limits. The federal government knew about contamination as early as the 1980s but delayed disclosure for years. The Camp Lejeune Justice Act of 2022 (part of the PACT Act) finally gave victims the right to sue the federal government — a right previously blocked by North Carolina's statute of repose. The administrative claim deadline under the CLJA was August 10, 2024, and is now closed for new claimants. However, tens of thousands of claimants filed timely administrative claims and are now engaged in litigation in the Eastern District of North Carolina, Wilmington Division. Our firm represents clients in that litigation and also assists veterans in filing and upgrading VA disability claims, which remain open regardless of the CLJA deadline.

Car Accident

Car accidents are the most common type of personal injury case in America. With over 6 million motor vehicle crashes reported annually by the National Highway Traffic Safety Administration, the insurance and legal landscape for MVA claims is vast and complex. Insurance companies spend billions each year on adjusters, defense attorneys, and claims management systems designed to reduce payouts to injured drivers, passengers, and pedestrians. Injuries range from relatively minor soft tissue damage like whiplash to catastrophic and life-altering conditions including traumatic brain injuries, spinal cord damage, and wrongful death. The legal systems governing fault — from pure comparative negligence in states like California to contributory negligence in Virginia — dramatically affect what injured parties can recover. Hiring an experienced car accident attorney is the single most impactful step an injured person can take to level the playing field against well-resourced insurance companies.

Catholic Church Abuse Lawsuit

Sexual abuse perpetrated by Catholic clergy — priests, deacons, brothers, bishops, and other Church officials — is one of the most extensively documented institutional abuse crises in American history. The 2002 Boston Globe Spotlight investigation exposed systemic cover-up by the Archdiocese of Boston, triggering a nationwide reckoning. Since then, over 30 dioceses have filed for bankruptcy protection and more than $4 billion in settlements have been paid to survivors across the United States. Today, many survivors who experienced abuse decades ago have renewed legal options through state lookback windows — temporary legislation that suspends the statute of limitations and opens a new filing period — and through diocesan bankruptcy claims processes with court-supervised compensation funds. California's lookback window is open through December 2027. Louisiana's window is open through June 2027. New York opens a new lookback window in March 2026. The Diocese of Alexandria's bankruptcy claims deadline is June 8, 2026. If you experienced abuse by a Catholic clergyman, speaking with an attorney now can clarify exactly what options remain available to you.

Coal Ash Contamination Lawsuit

Coal combustion residuals — commonly called coal ash — are the second-largest industrial waste stream in the United States, behind only mining waste. Every coal-fired power plant in the country produces coal ash, and the utility industry has disposed of it for decades by dumping it into unlined surface impoundments (wet ash ponds) and dry landfills, many of them sited directly above drinking water aquifers. The toxic constituents of coal ash — arsenic, hexavalent chromium, lead, mercury, selenium, cadmium, boron, and naturally occurring radioactive materials — migrate through soil into groundwater over time, especially from unlined ponds where water constantly percolates through the ash and carries dissolved metals into the subsurface. Duke Energy is the primary corporate defendant in coal ash contamination litigation. The company operates the largest fleet of coal-fired power plants in the United States and maintains more than 17 coal ash disposal sites in North Carolina alone. The North Carolina Department of Environmental Quality (DEQ) and independent testing have confirmed that groundwater at virtually all Duke Energy coal ash sites in the state exceeds safe drinking water standards for one or more heavy metals. Thousands of households near these sites rely on private wells — which are not subject to the public water supply testing requirements of the Safe Drinking Water Act — and many consumed contaminated water for years before the extent of the problem became known. The Tennessee Valley Authority (TVA), American Electric Power (AEP), Dominion Energy, and other major utilities face similar claims in their respective service territories. The legal landscape shifted dramatically after the 2014 Dan River spill, when a stormwater pipe beneath a Duke Energy coal ash pond at the retired Dan River Steam Station collapsed and released 39,000 tons of toxic ash and 27 million gallons of contaminated water into the Dan River. The disaster prompted federal criminal charges, a $102 million settlement, and the passage of North Carolina's Coal Ash Management Act requiring excavation of high-risk sites. The EPA finalized the Coal Combustion Residuals Rule in 2015 — the first-ever federal regulation of coal ash disposal — and strengthened it in 2024 to cover legacy surface impoundments that had previously been exempted. Individual plaintiffs in communities near coal ash sites are now pursuing cancer claims, medical monitoring, property damage, and diminished property value lawsuits against Duke Energy and other utilities.

Construction Accident Lawsuit

Construction is one of the most dangerous industries in America. The Bureau of Labor Statistics recorded 1,032 construction fatalities in 2024, and the Fatal Four — falls, struck-by accidents, electrocution, and caught-in/between accidents — account for 65% of all deaths on construction sites. For injured workers, workers' compensation covers medical bills and a portion of lost wages, but it does not pay for pain and suffering, and it caps your recovery at scheduled benefit amounts. If a third party — a general contractor, subcontractor, property owner, equipment manufacturer, or scaffolding rental company — contributed to your injury through negligence, you may have the right to file a civil lawsuit that recovers full damages on top of your workers' comp benefits. In New York, Labor Law §240, the 'Scaffold Law,' imposes absolute liability on property owners and general contractors for gravity-related construction accidents, making New York one of the strongest states in the country for injured construction workers. OSHA inspection records and violation citations against contractors are admissible as evidence of negligence in civil litigation. People's Justice helps injured construction workers navigate both the workers' comp system and the third-party civil lawsuit — the dual-track strategy that maximizes total recovery.

Demandas por Cáncer Asociado a Alisadores de Cabello

Los alisadores y tratamientos químicos para el cabello contienen sustancias químicas disruptoras endocrinas (EDC) — incluyendo ftalatos, parabenos, formaldehído y ciclosiloxanos — que imitan al estrógeno y alteran el sistema hormonal. El estudio Sister del NIH/NIEHS (2022) encontró que las mujeres que usaban frecuentemente estos productos enfrentaban más del doble de riesgo de cáncer uterino. Más de 14,700 demandas están consolidadas en el MDL 3060 en el Distrito Norte de Illinois, con juicios piloto esperados para 2027. El litigio masivo por daños afecta de manera desproporcionada a mujeres afrodescendientes, quienes fueron el principal objetivo de comercialización y representan aproximadamente el 60% de las usuarias afectadas.

Demandas por Efectos Secundarios de Ozempic y GLP-1

Los medicamentos agonistas del receptor GLP-1 — incluyendo Ozempic, Wegovy y Rybelsus de Novo Nordisk, y Mounjaro y Zepbound de Eli Lilly — han generado más de $40,000 millones en ventas anuales mientras presuntamente causan lesiones gastrointestinales graves que los fabricantes no revelaron adecuadamente. Más de 3,100 demandas están consolidadas en el MDL 3094 en el Distrito Este de Pensilvania ante la jueza Karen S. Marston. Los demandantes alegan que Novo Nordisk y Eli Lilly conocían la gravedad de las complicaciones gastrointestinales — incluyendo gastroparesis, obstrucción intestinal, pancreatitis y enfermedad de la vesícula biliar — pero no advirtieron adecuadamente a los pacientes ni a los médicos prescriptores. La FDA actualizó las advertencias sobre el riesgo de obstrucción intestinal en 2023. Los juicios piloto están programados para 2026, con selección de casos de prueba en curso.

Demandas por Fórmula Infantil y Enterocolitis Necrotizante (NEC)

La Enterocolitis Necrotizante es una de las enfermedades más catastróficas que afectan a los bebés prematuros en Estados Unidos, afectando aproximadamente al 12% de los bebés de muy bajo peso al nacer y con una tasa de mortalidad del 20-30%. La investigación médica que abarca más de dos décadas ha vinculado consistentemente la fórmula infantil a base de leche de vaca para prematuros — particularmente Similac Special Care (Abbott Laboratories) y Enfamil Premature (Mead Johnson/Reckitt) — con un riesgo dramáticamente elevado de NEC en bebés prematuros. Los estudios muestran que los bebés prematuros alimentados con fórmula a base de leche de vaca tienen de tres a diez veces más probabilidades de desarrollar NEC que aquellos alimentados con leche materna humana o leche materna pasteurizada de donante. A pesar de esta evidencia científica bien establecida y las recomendaciones de la American Academy of Pediatrics, Abbott y Mead Johnson continuaron comercializando agresivamente sus productos de fórmula en las NICU para su uso en la población de pacientes más vulnerable de la medicina. Miles de familias en todo el país han presentado demandas contra estos fabricantes, y los casos están ahora consolidados en el litigio masivo por daños (MDL 3026) en el Tribunal de Distrito de los Estados Unidos para el Distrito Norte de Illinois, ante la jueza Rebecca R. Pallmeyer. Las familias que perdieron a un bebé por NEC o cuyo bebé sobrevivió con daño duradero merecen respuestas, responsabilidad y compensación financiera por su pérdida.

Depo-Provera Brain Tumor Lawsuits

Depo-Provera (medroxyprogesterone acetate / MPA) is a contraceptive injection administered every three months. Over 2,000 lawsuits consolidated in MDL 3140 in the Northern District of Florida allege that Pfizer failed to warn about a significantly elevated risk of meningioma — a tumor in the tissue surrounding the brain and spinal cord. Women who received the shot for more than one year face up to a 5.6-fold increased risk, and the risk escalates with duration of use.

Elmiron Vision Loss Lawsuit

Interstitial cystitis (IC) is a chronic condition causing bladder pressure, bladder pain, and sometimes pelvic pain. It affects an estimated 3 to 8 million women and 1 to 4 million men in the United States. When the FDA approved pentosan polysulfate sodium — marketed as Elmiron — in 1996, it became the only oral medication specifically approved to treat IC symptoms. The drug works by helping to restore the glycosaminoglycan (GAG) layer that protects the bladder wall lining. Standard dosing is 100 mg taken three times daily, and because IC is a chronic condition, most patients take Elmiron for years or even decades. Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson, manufactures and markets the drug. For over two decades, Elmiron was considered safe for long-term use. That changed in 2018 when Dr. Nieraj Jain and colleagues at Emory University published groundbreaking research identifying a distinctive pattern of retinal damage in long-term Elmiron users. The condition, now called pentosan polysulfate maculopathy or pigmentary maculopathy, involves toxic damage to the retinal pigment epithelium (RPE) and photoreceptor cells. This unique pattern of injury was frequently misdiagnosed as age-related macular degeneration before the Emory team identified the connection to Elmiron. Subsequent studies confirmed a clear dose-dependent relationship: patients who took more Elmiron over longer periods suffered worse eye damage. Research published in peer-reviewed journals found prevalence rates ranging from roughly 13 percent in patients with moderate cumulative exposure to over 40 percent in those with the highest exposure levels. In June 2020, the FDA required Janssen to update Elmiron's prescribing label to include warnings about retinal pigmentary changes. Janssen and J&J maintained that the drug was safe when used as directed. Lawsuits began consolidating in 2020 into MDL 2973 in the District of New Jersey under Judge Brian R. Martinotti. At its peak, nearly 2,000 cases were filed. As of February 2026, approximately 640 cases remain pending as the litigation winds toward resolution. Some cases have settled confidentially, and legal experts anticipate a broader settlement in the near future. The declining case count reflects both ongoing settlements and case consolidation rather than a lack of merit.

Ethylene Oxide

Ethylene oxide (EtO) is a highly toxic chemical used to sterilize medical equipment and manufacture other chemicals. The EPA determined in 2016 that EtO is carcinogenic to humans at exposure levels far lower than previously thought. Residents living near EtO-emitting facilities in Georgia, Illinois, Texas, Colorado, and other states have filed lawsuits alleging their cancers — including lymphoma, breast cancer, and leukemia — were caused by chronic exposure to EtO emissions.

Exactech Knee Recall

Exactech Inc. manufactured knee replacement implants with defective packaging that lacked an inner oxygen barrier, causing polyethylene liners to degrade before implantation. The resulting premature implant failures led to a 2022 recall covering ~147,000 US patients. Lawsuits allege Exactech and parent company TPG Capital knew of the packaging defect and failed to warn surgeons and patients. The primary remedy — revision surgery — is a major operation with serious complication risks.

Hair Relaxer Cancer Lawsuits

Chemical hair relaxers and straighteners contain endocrine-disrupting chemicals (EDCs) — including phthalates, parabens, formaldehyde, and cyclosiloxanes — that mimic estrogen and disrupt the hormonal system. The NIH/NIEHS Sister Study (2022) found that women who frequently used these products faced more than double the risk of uterine cancer. Over 14,700 lawsuits are consolidated in MDL 3060 in the Northern District of Illinois, with bellwether trials expected in 2027. The litigation disproportionately affects Black women, who were the primary marketing target and comprise approximately 60% of affected users.

Hernia Mesh (Davol/C.R. Bard)

Hernia mesh litigation is one of the largest ongoing mass tort actions in the United States. Polypropylene mesh devices implanted during inguinal, ventral, and incisional hernia repairs have been associated with a pattern of serious defects — including mesh shrinkage, migration, erosion into adjacent organs, bacterial colonization, and nerve entrapment — that manufacturers knew about for years before disclosing to physicians or patients. The primary defendants include Davol Inc. and its parent C.R. Bard (now part of Becton Dickinson), Ethicon (a Johnson and Johnson subsidiary), Atrium Medical, and Covidien (now part of Medtronic). The federal multidistrict litigation MDL 2846 in the Southern District of Ohio has consolidated thousands of Davol/C.R. Bard claims for coordinated pre-trial proceedings. Separately, Ethicon mesh cases are coordinated in New Jersey Superior Court (MCL 616). Patients who underwent hernia repair surgery and subsequently experienced complications are urged to seek legal evaluation immediately — statutes of limitations are running and evidence must be preserved.

IVC Filter

Retrievable IVC filters manufactured by C.R. Bard and Cook Medical have failed at alarming rates — fracturing, migrating to the heart, and perforating organs. Two federal MDLs are actively resolving thousands of claims. Bard has entered a confidential global settlement program; Cook cases proceed individually. Free consultations available.

Instant Soup Burns

Instant soup products designed in cup or bowl form are a staple of American households, yet their design creates a foreseeable and recurring hazard: scalding liquid spills onto consumers when the lightweight cup tips or collapses. Children under five are disproportionately affected because they are more likely to encounter unattended cups of hot soup at table or counter height and because their skin is thinner and more vulnerable to deep burns at lower temperatures and shorter contact durations. Product liability law allows burn victims to sue manufacturers under three distinct theories — design defect, manufacturing defect, and failure to warn — without needing to prove the company acted with any particular intent. The CPSC has received hundreds of burn injury reports related to instant cup soups. An experienced product liability attorney can hold manufacturers accountable and recover compensation for medical treatment, scarring, pain and suffering, and in child cases, the long-term emotional and cosmetic impact of permanent disfigurement.

Juvenile Detention Center Abuse

The abuse of children in juvenile detention is a national crisis. Across the United States, approximately 36,000 young people are held in juvenile detention facilities, youth correctional centers, and residential treatment programs on any given day. Federal surveys by the Bureau of Justice Statistics found that more than 10% of confined youth report sexual victimization — and more than 80% of that abuse is perpetrated by staff, not other detainees.

LDS Church Abuse

The Church of Jesus Christ of Latter-day Saints (LDS Church) faces mounting lawsuits from survivors of sexual abuse by clergy, leaders, and members. At the center of the litigation is the Church's internal "help line" — a hotline staffed by attorneys that, according to lawsuits, was used to manage legal liability rather than protect children. Survivors allege the Church systematically failed to report abuse to authorities, moved known abusers to new congregations, and discouraged victims from going to police.

Medical Malpractice

Medical malpractice litigation is among the most technically demanding areas of personal injury law, requiring attorneys and clients to navigate complex medical evidence, expert witness requirements, and state-specific procedural hurdles like certificates of merit and notice of intent requirements. The stakes are enormous: a surgical error can leave a patient permanently disabled, a missed cancer diagnosis can allow a curable disease to become terminal, and a birth injury can alter an entire family's life trajectory. The Journal of the American Medical Association (JAMA) has published studies suggesting that medical errors are the third leading cause of death in the United States. Yet fewer than 2% of patients harmed by negligence ever file a claim, often because they do not know they have rights or cannot find an attorney willing to take on the complexity and cost of malpractice litigation. People's Justice exists to change that equation — connecting injured patients and families with experienced medical malpractice attorneys who work on contingency with no upfront cost.

NEC Baby Formula (Similac/Enfamil)

Necrotizing Enterocolitis is one of the most catastrophic diseases affecting premature infants in the United States, striking approximately 12% of very-low-birthweight babies and carrying a mortality rate of 20-30%. Medical research spanning more than two decades has consistently linked cow's milk-based premature infant formula — particularly Similac Special Care (Abbott Laboratories) and Enfamil Premature (Mead Johnson/Reckitt) — to dramatically elevated NEC risk in preterm infants. Studies show that premature infants fed cow's milk-based formula are three to ten times more likely to develop NEC than those fed human breast milk or pasteurized donor breast milk. Despite this well-established scientific evidence and the recommendations of the American Academy of Pediatrics, Abbott and Mead Johnson continued to aggressively market their formula products to NICUs for use in the most vulnerable patient population in medicine. Thousands of families across the country have filed suit against these manufacturers, and the cases are now consolidated in Multi-District Litigation (MDL 3026) in the United States District Court for the Northern District of Illinois, before the Honorable Rebecca R. Pallmeyer. Families who lost a baby to NEC or whose infant survived with lasting harm deserve answers, accountability, and financial compensation for their loss.

Nursing Home Abuse & Elder Abuse

Nursing home abuse is a pervasive crisis affecting the most vulnerable members of our society. Approximately 1.5 million Americans reside in nursing homes and long-term care facilities, and a significant proportion experience some form of abuse, neglect, or exploitation. The federal government regulates nursing home quality through the Centers for Medicare and Medicaid Services (CMS), which publishes a five-star rating system and conducts regular health inspections — yet facilities with poor ratings continue to operate, understaffed and underfunded, leaving residents at serious risk. Types of abuse range from physical assault and sexual abuse to financial exploitation, emotional cruelty, and systematic neglect of basic care needs. When nursing homes and assisted living facilities breach their legal duty of care, they can be held liable for the full range of damages suffered by residents and their families, including medical expenses, pain and suffering, emotional distress, and in egregious cases, punitive damages designed to deter future misconduct.

Olympus Duodenoscope Lawsuit

Endoscopic retrograde cholangiopancreatography (ERCP) is a procedure performed roughly 500,000 times per year in the United States. It uses a specialized endoscope called a duodenoscope to visualize and treat conditions of the bile ducts and pancreas — including gallstones, tumors, and blockages. Olympus Corporation has dominated the duodenoscope market for decades, holding an estimated 85 percent or more of the U.S. market share. The Olympus TJF-Q180V and its successor models (TJF-Q190V, TJF-Q290V) feature a movable elevator mechanism at the distal tip that allows physicians to precisely manipulate guidewires and instruments during the procedure. That elevator mechanism is at the heart of a design defect that has infected hundreds of patients with deadly superbug bacteria. The elevator's sealed channel creates microscopic crevices where tissue, blood, and bacteria become trapped during procedures. These crevices cannot be adequately cleaned using the reprocessing (sterilization) methods specified by Olympus — a fact the company has now acknowledged in multiple safety notices. The bacteria that survive reprocessing include carbapenem-resistant Enterobacteriaceae (CRE), which the CDC has classified as a nightmare bacteria because it resists nearly all available antibiotics and carries a mortality rate of 40 to 50 percent in bloodstream infections. Superbug outbreaks linked to Olympus duodenoscopes have been documented at more than 40 hospitals worldwide, including UCLA Ronald Reagan Medical Center, Virginia Mason Medical Center in Seattle, Cedars-Sinai Medical Center, and Advocate Lutheran General Hospital. The FDA has issued multiple safety communications, required post-market surveillance, and in 2021 recommended that all healthcare facilities transition to duodenoscopes with disposable components or fully disposable models. In October 2025, Olympus issued yet another Urgent Field Safety Notice admitting that reprocessing remains inadequate and recommending 10x magnification inspection of device tips. Litigation against Olympus began in 2015 and has included individual lawsuits, hospital claims, and wrongful death actions. The primary defendants are Olympus Corporation (Tokyo) and Olympus Corporation of the Americas.

Ozempic / GLP-1 Lawsuits

GLP-1 receptor agonist drugs — including Novo Nordisk's Ozempic, Wegovy, and Rybelsus, and Eli Lilly's Mounjaro and Zepbound — have generated over $40 billion in annual sales while allegedly causing severe gastrointestinal injuries that manufacturers failed to adequately disclose. Over 3,100 lawsuits are consolidated in MDL 3094 in the Eastern District of Pennsylvania, with a separate NAION vision-loss MDL (3163) established in December 2025.

PFAS Water Contamination Lawsuit

PFAS (per- and polyfluoroalkyl substances) are a group of more than 12,000 synthetic chemicals that have been used in manufacturing since the 1940s. They are called 'forever chemicals' because they do not break down in the environment or in the human body. PFAS were used extensively in aqueous film-forming foam (AFFF), the firefighting foam used at military bases and airports for decades. PFAS-contaminated AFFF has leached into groundwater near hundreds of military installations and civilian airports across the United States. PFAS were also discharged into waterways by industrial manufacturers — most notably DuPont's PFOA contamination of the Ohio River valley and Chemours' GenX contamination of the Cape Fear River in North Carolina. 3M manufactured PFOS-based PFAS and supplied them to the military and industry from the 1950s through 2002. Both companies concealed internal studies showing that PFAS accumulated in human blood and were linked to cancer. MDL 2873 — the AFFF Products Liability Litigation in the District of South Carolina — consolidates individual personal injury claims. The 3M water system settlement ($12.5B, 2023) and the DuPont/Chemours/Corteva water system settlement ($1.185B, 2024) have resolved municipal water utility claims but left individual personal injury claims unresolved. Individuals diagnosed with kidney cancer, testicular cancer, thyroid cancer, thyroid disease, ulcerative colitis, or other PFAS-linked conditions following documented exposure to contaminated drinking water may have significant individual claims.

Paragard IUD Lawsuit

Paragard (T380A copper IUD) was FDA-approved in 1984 and has been used by millions of American women as a hormone-free long-term contraceptive. Women and their doctors began reporting a troubling pattern: when Paragard is removed — a routine office procedure — the device's copper-and-plastic arms snap off inside the patient. The retained fragments can migrate, perforate organs, cause chronic pelvic pain, and require invasive surgery including hysteroscopy, laparoscopy, and in some cases hysterectomy to remove. Women who suffered uterine perforation, organ damage, or infertility from a broken Paragard may have a product liability claim against Teva Pharmaceuticals. The MDL is pending before Judge Leigh Martin May in the Northern District of Georgia. The first bellwether trial (Rickard v. Teva) ended in a defense verdict on February 5, 2026. Two additional bellwether trials are scheduled in March and May 2026. Settlement negotiations are active. Claimants who can document breakage, surgery, and significant injury — especially infertility — have the strongest cases.

Paraquat Parkinson’s

Paraquat is a restricted-use herbicide manufactured primarily by Syngenta and distributed by Chevron Phillips Chemical and Growmark. Despite being banned in more than 70 countries including the European Union, China, Brazil, and Thailand, paraquat remains legal in the United States, where approximately 10 million pounds are applied annually. Scientific evidence — including the landmark Farming and Movement Evaluation (FAME) study published in 2011 — demonstrates that paraquat exposure increases the risk of Parkinson’s disease by 2.5 times. The mechanism is well understood: paraquat triggers oxidative stress through redox cycling, inhibits mitochondrial complex I, and selectively kills dopamine-producing neurons in the substantia nigra, leading to the progressive motor and cognitive deterioration characteristic of Parkinson’s disease. MDL 3004 was established in June 2021 in the Southern District of Illinois, with approximately 5,000 cases pending. Bellwether proceedings and settlement negotiations are ongoing, with projected individual settlements ranging from $20,000 to over $1,000,000 depending on disease severity and exposure documentation.

Rideshare Sexual Assault (Uber/Lyft)

Every ride requested through a rideshare app comes with an implicit promise of safety. When Uber and Lyft fail to fulfill that promise — through inadequate background checks, failure to remove dangerous drivers, or systemic indifference to survivor reports — the companies bear legal responsibility for the harm survivors experience. Uber's 2022 U.S. Safety Report, released only after sustained legal and public pressure, disclosed 3,824 reports of sexual assault in just two years of rides. Advocacy organizations and litigation experts believe those numbers dramatically undercount the true scope because most survivors never report to Uber or Lyft, let alone law enforcement. Both companies now face consolidated multi-district litigation (MDL) proceedings — Uber in the Northern District of California, Lyft in the same court — where thousands of individual claims have been joined for pre-trial proceedings. Civil litigation against rideshare platforms is separate from and independent of any criminal case, and survivors can pursue civil claims regardless of whether a criminal prosecution occurred or resulted in conviction. An experienced rideshare sexual assault attorney can evaluate your case confidentially, explain your rights, and pursue maximum compensation with complete discretion.

Roblox Child Exploitation

Roundup

Roundup, the world’s most widely used herbicide, contains glyphosate — a chemical the World Health Organization classified as "probably carcinogenic to humans" in 2015. Monsanto, which created Roundup, was acquired by Bayer in 2018. Internal documents revealed Monsanto knew of cancer risks but chose to suppress the science and attack independent researchers. Juries have awarded billions in damages, and Bayer has paid over $11 billion in settlements.

Slip and Fall Lawsuit

Slip and fall accidents — legally categorized as premises liability claims — occur when a property owner's failure to maintain safe conditions causes someone to fall and suffer injuries. Property owners and managers have a legal duty to inspect their property, identify hazardous conditions, and either fix them or warn visitors. When they fail that duty, injured victims may recover compensation for medical bills, lost wages, pain and suffering, and long-term disability. Commercial properties — including grocery stores, restaurants, parking lots, and retail chains — average $345,000 in premises liability settlements nationally. Private property cases average $105,000. Cases involving spinal cord injuries, traumatic brain injury, or surgical intervention command significantly higher values. Government property claims present a unique complication: injury victims often have only 30 to 90 days to file a formal notice of claim with the government entity before losing their right to sue entirely. An attorney should be contacted immediately after any fall on public property.

Social Media Addiction

Social media addiction among children and adolescents has reached crisis proportions in the United States, with the U.S. Surgeon General issuing two consecutive advisories identifying social media as a driving force behind the youth mental health epidemic. An estimated 95% of teens ages 13-17 use social media, with more than a third reporting they use it "almost constantly." The platforms at the center of this litigation — Instagram, TikTok, Snapchat, YouTube, and Facebook — are precision-engineered behavioral systems that exploit developing brains through algorithmic content amplification, infinite scroll, autoplay, streaks, beauty filters, and notification systems designed to maximize engagement at any cost. Research shows that teens spending 3+ hours per day on social media face double the risk of anxiety and depression. MDL 3047 has consolidated over 1,600 cases, and the K.G.M. bellwether trial began in February 2026.

Storm Damage Lawsuit

Storm damage insurance claims represent one of the fastest-growing areas of property insurance litigation in the United States. Every year, hurricanes, tornadoes, hailstorms, and flooding events cause tens of billions of dollars in property damage, and millions of homeowners and business owners file insurance claims expecting their policies to cover the cost of repairs. The reality is far more difficult. Insurance companies routinely deny, delay, and underpay storm damage claims using a range of tactics, from blaming pre-existing damage to classifying structural harm as merely cosmetic. In 2024, Hurricane Helene struck the Southeast as a Category 4 storm, causing over $80 billion in damage, while Hurricane Milton caused an additional $17 to $28 billion in insured losses in Florida. Denial rates for hurricane claims reached 33 percent for Helene and 41 percent for Milton. The 2025 tornado season brought $89 billion in losses across the central United States, and the LA fires caused $107 billion in damage in a state already facing an insurance crisis. What makes storm damage claims different from other property claims is the sheer scale of destruction and the insurance industry's systemic response. After major disasters, insurers face thousands of simultaneous claims and adopt aggressive cost-containment strategies that prioritize their bottom line over policyholders' needs. They deploy preferred vendors who produce low repair estimates, use desk adjusters who never inspect the property, and invoke policy exclusions that may not actually apply. Policyholders who fight back, either through the appraisal process or through bad faith litigation, consistently recover significantly more than those who accept the insurer's initial offer. An experienced storm damage attorney helps level the playing field by documenting the full scope of damage, challenging improper denials, and holding insurers accountable when they act in bad faith.

Suboxone Tooth Decay

Suboxone sublingual film strips — a medication-assisted treatment (MAT) for opioid use disorder — dissolve under the tongue and contain citric acid and other acidic excipients that, with repeated use, erode tooth enamel and cause rapid, severe dental decay. Thousands of patients who faithfully took Suboxone as prescribed to manage opioid dependence later discovered they had lost multiple teeth, required extensive dental reconstruction, or faced thousands of dollars in oral surgery costs — through no fault of their own. Manufacturer Indivior (formerly part of Reckitt Benckiser) knew or should have known about these dental risks for years but failed to include adequate warnings on the product label. The FDA confirmed the danger with a formal safety communication on January 12, 2022, requiring updated product labeling. Patients who suffered dental injuries while using Suboxone sublingual film may have valid product liability claims against Indivior for failure to warn.

Talcum Powder

Talcum powder litigation is one of the largest and most consequential mass tort actions in American history. More than 63,000 lawsuits have been filed against Johnson & Johnson and its talc supplier Imerys, alleging that decades of Baby Powder use caused ovarian cancer, mesothelioma, and other cancers. The litigation centers on two distinct but related harms: the carcinogenic properties of talc itself when applied to the perineal area, and asbestos contamination in talc products traced to mining operations. Juries across the country have returned billions of dollars in verdicts, including a $4.69 billion verdict in St. Louis (later reduced to $2.12 billion on appeal) and a $1.56 billion verdict in Baltimore in December 2025. J&J discontinued talc-based Baby Powder in North America in 2020 and globally in 2022, replacing it with cornstarch. The MDL 2738 in the District of New Jersey, now before Judge Michael Shipp, is coordinating federal proceedings with bellwether trials underway.

Tepezza Hearing Loss Lawsuit

Thyroid eye disease (TED), also called Graves' ophthalmopathy, is an autoimmune condition that causes the muscles and fatty tissue behind the eyes to swell, leading to eye bulging (proptosis), double vision, pain, and in severe cases vision loss. TED affects an estimated 16,000 Americans per year and is closely associated with Graves' disease, an overactive thyroid condition. Before Tepezza, treatment options were limited to steroids, orbital radiation, and surgery. Teprotumumab, sold under the brand name Tepezza, is a monoclonal antibody that works by blocking insulin-like growth factor 1 receptor (IGF-1R). The FDA granted Tepezza Breakthrough Therapy designation and approved it in January 2020, making it the first and only FDA-approved medication specifically for TED. It is administered as a series of eight intravenous infusions over approximately 21 weeks. Horizon Therapeutics, a Dublin-based pharmaceutical company, developed and marketed Tepezza. In December 2023, Amgen completed its acquisition of Horizon Therapeutics for $27.8 billion, assuming responsibility for the Tepezza product line and its associated liabilities. At roughly $300,000 per treatment course, Tepezza is one of the most expensive drugs in the United States. The hearing damage mechanism centers on the role of IGF-1R in the inner ear. IGF-1R is expressed in cochlear hair cells, where it supports cell survival, prevents programmed cell death, and promotes the regeneration of cochlear synapses. By blocking IGF-1R throughout the body — not just in the eye orbit — Tepezza may deprive inner ear hair cells of critical survival signaling, leading to sensorineural hearing loss, tinnitus, autophony, and eustachian tube dysfunction. Clinical trial data submitted to the FDA showed hearing impairment in 10% of Tepezza patients compared to 0% on placebo, but these rates were based on limited study populations. A 2021 Endocrine Society prospective study found that 65% of patients experienced audiometric changes after treatment. The FDA required label changes in July 2023 acknowledging that hearing loss from Tepezza may be severe and permanent. The MDL was formed in June 2023 and assigned to Judge Thomas M. Durkin in the Northern District of Illinois. The first lawsuit was filed in 2022. As of early 2026, 273 cases are pending with 282 total filed. Active litigation continues.

Testosterone Therapy

Men who used AndroGel, Axiron, Androderm, or other testosterone replacement products and suffered cardiovascular injuries — including heart attack, stroke, or blood clots — may qualify for compensation through MDL 2545 or individual state court litigation.

Transvaginal Mesh

Surgical mesh implanted transvaginally to treat pelvic organ prolapse and stress urinary incontinence caused widespread injuries including erosion, chronic pelvic pain, and the need for revision surgery. Six MDLs were consolidated before Judge Joseph Goodwin in the Southern District of West Virginia. Major manufacturers paid over $1.9 billion in global settlements. Individual cases remain active, especially for women who recently connected their symptoms to their mesh implant.

Truck / 18-Wheeler Accident

Truck accident claims are far more complex than standard car accident cases. The Federal Motor Carrier Safety Administration (FMCSA) imposes strict regulations on commercial carriers — hours-of-service limits, mandatory drug testing, electronic logging device (ELD) requirements, and vehicle inspection protocols — and violations of these rules are powerful evidence of negligence. Trucking companies carry commercial liability insurance of $750,000 to $5 million depending on cargo type, making higher recoveries possible. Multiple parties may be liable: the truck driver, the motor carrier, the cargo loader, the freight broker, and vehicle or parts manufacturers. Black box data (EDR), ELD records, GPS tracking, and driver qualification files are critical evidence that must be preserved immediately after the crash. Victims who act quickly to retain experienced truck accident counsel — and who send spoliation letters before data is destroyed — consistently achieve far better outcomes than those who wait.

Tylenol Autism Lawsuit

Acetaminophen — sold under the brand name Tylenol by Kenvue (formerly Johnson & Johnson) and as dozens of store-brand generics by Walmart, CVS, Walgreens, Target, Costco, Meijer, and others — was the most commonly used pain reliever during pregnancy in the United States for decades. Starting with a landmark 2018 American Journal of Epidemiology meta-analysis of 130,000 mother-child pairs, and culminating in a 2021 consensus statement signed by 91 scientists published in Nature Reviews Endocrinology, accumulating evidence linked prolonged prenatal acetaminophen exposure to significantly elevated risks of autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (ADHD). The federal multidistrict litigation, MDL-3043 (In re Acetaminophen — ASD/ADHD Products Liability Litigation) in the Southern District of New York, was dismissed in August 2024 after Judge Denise L. Cote excluded all plaintiffs' general causation experts under the Daubert standard. Critically, the Second Circuit Court of Appeals heard oral arguments on November 17, 2025 — and two of the three judges on the panel openly questioned whether Judge Cote acted too aggressively in excluding the expert testimony. A reversal by the Second Circuit could reinstate thousands of federal cases. Separately, California state courts (Alameda County) and Illinois state courts (St. Clair, Madison, and Cook counties) have active acetaminophen-autism cases proceeding under the Frye admissibility standard, which does not apply the same gatekeeping test that closed the federal MDL. Store-brand acetaminophen users have the same legal claims as Tylenol brand users — the failure-to-warn theory applies equally to Walmart's Equate brand, CVS Health brand, Walgreens brand, Costco Kirkland brand, and all other private-label acetaminophen products.

Video Game Addiction

Video game addiction among children and adolescents has reached crisis proportions in the United States, with the World Health Organization formally classifying Gaming Disorder as a medical condition in 2019. An estimated 91% of American children ages 2 to 17 play video games, and research shows that between 3% and 10% of youth gamers meet clinical criteria for addiction. The games at the center of this litigation are precision-engineered behavioral systems that employ variable-ratio reinforcement schedules found in slot machines. Loot boxes, battle passes, and engagement-optimized matchmaking are designed to create compulsive use in children. The FTC’s $520 million settlement with Epic Games established federal precedent, and hundreds of individual lawsuits have been consolidated for coordinated proceedings with bellwether trials expected in 2026.

Wildfire Damage Lawsuit

The wildfire crisis in America is accelerating. Climate change has extended fire seasons by months, extreme drought has left landscapes tinder-dry, and decades of development in the wildland-urban interface have placed millions of homes directly in the path of fire. Utility-caused fires have been responsible for some of the worst disasters in recent memory. PG&E's faulty transmission line sparked the 2018 Camp Fire in Paradise, California, killing 85 people and destroying nearly 19,000 structures. PG&E ultimately pled guilty to 84 counts of involuntary manslaughter and paid $13.5 billion to wildfire victims before entering bankruptcy. Southern California Edison has paid over $2 billion to settle claims from the Woolsey Fire and Thomas Fire. Xcel Energy faces lawsuits over the 2021 Marshall Fire in Colorado, and Hawaii Electric is being sued for the 2023 Maui fire that killed over 100 people. At the same time, the insurance industry is retreating from fire-prone regions. State Farm and Allstate have stopped writing new homeowner policies in California, leaving residents scrambling for coverage through the FAIR Plan — the insurer of last resort. Wildfire victims who do have coverage frequently encounter disputes over replacement cost versus actual cash value, underinsurance gaps where rebuilding costs far exceed policy limits, and delays in additional living expense payments. The legal framework for wildfire claims includes inverse condemnation in California, which holds utilities strictly liable when their equipment damages private property, as well as traditional negligence, strict liability, and wrongful death claims. Victims may also have insurance bad faith claims against carriers that unreasonably deny or delay legitimate claims. Recent settlements demonstrate the substantial recoveries available to wildfire victims who pursue their legal rights.

Women’s Detention Abuse

Wrongful Death Lawsuit

A wrongful death lawsuit allows surviving family members to recover compensation when a loved one dies due to another party's negligence, recklessness, or intentional wrongdoing. These cases arise from car and truck accidents, medical malpractice, workplace incidents, nursing home abuse, and defective products. Recoverable damages include lost income the deceased would have earned, medical and funeral expenses, and the family's grief and loss of companionship. State laws control who may file (typically spouse, children, and parents), how long families have to file (1–3 years from the date of death in most states), and whether damages caps limit recovery. Texas imposes no cap on wrongful death damages, while Florida caps non-economic damages at $500,000 in medical malpractice cases. Illinois courts have struck down caps as unconstitutional. The distinction between a wrongful death claim and a survival action — the latter compensating the estate for the decedent's own pre-death suffering — is a critical legal issue that affects both strategy and potential recovery.

Zantac / Ranitidine (NDMA Cancer)

Ranitidine, sold under the brand name Zantac by Sanofi and previously by GSK, Pfizer, and Boehringer Ingelheim, was one of the most prescribed heartburn and acid reflux medications in history. In 2019, the independent pharmaceutical testing laboratory Valisure discovered that ranitidine is inherently unstable and produces NDMA — N-nitrosodimethylamine, a probable human carcinogen — at levels up to 304,500 nanograms per tablet. The FDA acceptable daily intake limit for NDMA is 96 nanograms. In April 2020, the FDA requested that all manufacturers withdraw ranitidine products from the U.S. market. Consumers who took Zantac regularly for a year or more and subsequently developed bladder, stomach, colorectal, breast, prostate, or esophageal cancer may have viable legal claims. A federal MDL in the Southern District of Florida was dismissed in November 2022 when Judge Robin Rosenberg excluded plaintiffs' general causation experts under Daubert, finding their methodologies unreliable. However, that ruling applies only to federal court and does not bind state courts. Litigation continues in Delaware Superior Court and California state courts in 2026, where different expert standards and case-specific evidence can support claims.

Zug Island Pollution Lawsuit

Zug Island — a 188-acre industrial complex at the southern tip of River Rouge, Michigan — has been one of the most polluted sites in the Great Lakes region for over a century. The EES Coke Battery facility, operated by a subsidiary of DTE Energy, produces metallurgical coke by heating coal to extreme temperatures in massive ovens. This coking process releases sulfur dioxide, particulate matter, hydrogen sulfide, and polycyclic aromatic hydrocarbons into the air. For years, the facility's SO2 emissions far exceeded the limits set by its Clean Air Act permits, exposing tens of thousands of Downriver residents to dangerous concentrations of toxic pollution. The health consequences have been devastating. Sulfur dioxide is a potent respiratory irritant that triggers asthma attacks, aggravates COPD and chronic bronchitis, and causes inflammation of the airways even at relatively low concentrations. Long-term exposure to elevated SO2 levels is associated with increased risk of cardiovascular disease, including heart attacks and strokes. The particulate matter and PAHs co-emitted by the coking process compound these risks, creating a toxic cocktail that has driven respiratory and cardiovascular disease rates in Downriver communities well above state and national averages. Children, the elderly, and people with pre-existing respiratory conditions are especially vulnerable. The February 2026 EPA enforcement action — a $100 million penalty plus $20 million in community benefit funds — represents the federal government's recognition that DTE Energy's Zug Island operations have caused serious harm to an environmental justice community. The penalty is among the largest ever assessed under the Clean Air Act. But a government fine, no matter how large, does not compensate individual residents for the asthma, COPD, heart disease, and other conditions they developed from breathing Zug Island's emissions for years or decades. Individual personal injury lawsuits offer a path to direct compensation for medical expenses, pain and suffering, lost wages, and diminished quality of life caused by this exposure.