Open Lawsuits & Class Actions

Smokers and former smokers diagnosed with lung cancer, COPD, or other tobacco-related diseases may be owed money. Cases now being filed in Oregon, Hawaii, New Mexico, Nevada, Massachusetts, and Illinois.

Patients who developed serious drug-resistant infections — including antibiotic-resistant CRE bacteria — after a hospital scope procedure may have a case against the manufacturer.

Families of children born with cerebral palsy, HIE, Erb's palsy, or other serious birth injuries caused by medical error during labor and delivery may be owed significant money.

Parents of premature babies who developed NEC — whether from formula, hospital negligence, or a NICU staff error — may have a case against the responsible party.

Survivors of sexual abuse at schools, churches, sports organizations, or other institutions may be able to file a civil case — even if the abuse happened decades ago.

If a doctor, hospital, or medical provider made a serious mistake that caused lasting injury or death, you may be owed money. Free review, no fees unless you win.

Injured by a defective firework or at a negligent firework display? You may be owed money for medical bills, lost income, and lasting harm. Free case check.

Women who used chemical hair relaxers or straighteners — including Dark & Lovely, ORS Olive Oil, Just for Me, or Motions — and were later diagnosed with uterine cancer, ovarian cancer, or endometriosis may qualify.

Firefighters, military personnel, and people who lived near airports or military bases who were regularly exposed to AFFF (aqueous film-forming foam) and developed kidney, testicular, thyroid, or bladder cancer may qualify.

Veterans, family members, or civilian workers who lived or worked at Camp Lejeune in North Carolina for at least 30 days between August 1953 and December 1987, and later developed cancer, Parkinson's disease, or leukemia, may qualify.

People who used Roundup weedkiller at home, on a farm, or at work and were diagnosed with non-Hodgkin lymphoma may qualify. A class settlement proposed by Bayer received preliminary court approval in March 2026.

Women who regularly used Johnson & Johnson Baby Powder or Shower to Shower in the genital area and were later diagnosed with ovarian cancer or mesothelioma may qualify. Over 67,000 cases remain pending after J&J's bankruptcy plan was rejected.

Farmers, landscapers, and agricultural workers who were regularly exposed to paraquat (Gramoxone) and were later diagnosed with Parkinson's disease may qualify. A settlement in principle has been reached and Syngenta has announced it will stop making the chemical.

Women who used Depo-Provera (medroxyprogesterone acetate) for a year or more and later developed a meningioma brain tumor may qualify. The FDA updated the Depo-Provera warning label in December 2025. More than 3,490 cases are pending in an MDL in the Northern District of Florida.

Parents of children diagnosed with autism or ADHD whose mothers took Tylenol (acetaminophen) regularly while pregnant may qualify. State court cases are actively being filed while a federal appeals court considers reviving the federal case.

People who took Ozempic, Wegovy, Mounjaro, or similar GLP-1 drugs and developed gastroparesis (stomach paralysis), severe vomiting, or required hospitalization for stomach or intestinal injuries may qualify.

People who took Zantac or generic ranitidine for extended periods and were diagnosed with stomach, bladder, or colorectal cancer may qualify. State court cases remain active following a Delaware Supreme Court review order.

Families of premature infants who were fed cow's-milk-based hospital formula — including Abbott's Similac or Mead Johnson's Enfamil — in the NICU and developed NEC (necrotizing enterocolitis), a serious bowel disease, may qualify.

Patients who took Elmiron (pentosan polysulfate sodium) for interstitial cystitis — a painful bladder condition — and developed vision problems or unexplained damage to the center of the retina (maculopathy) may qualify.

Patients who received Tepezza infusions for thyroid eye disease and afterward developed permanent hearing loss or ringing in the ears (tinnitus) — a risk not adequately disclosed before treatment — may qualify.

People who took Ozempic, Wegovy, Mounjaro, or other GLP-1 drugs and experienced sudden, permanent vision loss (NAION) may qualify. A federal court hearing on the science is set for June 2026. This is separate from the stomach paralysis lawsuit.

People who used a recalled Philips Respironics CPAP, BiPAP, or ventilator machine — recalled in 2021 because the foam could break down and release toxic particles — and were diagnosed with cancer or a serious lung condition may qualify.

People who had hernia surgery using a synthetic mesh from brands including Bard (Davol) or Covidien, and later experienced mesh migration, chronic pain, infection, or needed additional surgeries to fix the mesh, may qualify.

Patients who had a Cook Medical IVC (inferior vena cava) filter implanted to catch blood clots, and the filter later broke apart, moved inside the body, or caused organ damage or serious injury, may qualify. Nearly 7,000 cases remain pending.

Patients who received a recalled Exactech hip, knee, or ankle replacement implant — recalled due to defective packaging that damaged the plastic components — and experienced early device failure, bone loss, or needed repeat surgery may qualify.

Cancer patients and others who had a Bard PowerPort implanted catheter that fractured inside the body — sending plastic fragments toward the heart or lungs — may qualify. First federal trial began April 21, 2026. Over 3,200 cases pending.

Current and former AT&T customers whose personal information — including Social Security numbers, account passcodes, and call records — was exposed in the 2024 AT&T data breaches may qualify. A $177 million settlement is under court review.

Patients and healthcare workers whose medical or personal information was exposed in the February 2024 cyberattack on Change Healthcare — the largest healthcare data breach in U.S. history, affecting approximately 190 million people — may qualify.

People whose personal information — Social Security numbers, health records, or financial data — was exposed because a hospital, agency, or company they trusted used the MOVEit file transfer software hacked in May 2023 may qualify.

Owners or lessees of certain 2011–2022 Kia or Hyundai vehicles without standard engine immobilizers that were stolen or damaged following the viral "Kia Boyz" theft trend may qualify. A settlement claims window is open through March 2027.

Owners of 1999–2016 Ford Super Duty F-250, F-350, or F-450 trucks with allegedly weak roofs, or people injured — and families of those killed — in a rollover crash where the roof collapsed, may qualify for individual injury cases being actively filed.

Owners of 2020–2023 Ford Bronco Sport or Ford Maverick vehicles with 1.5-liter engines who experienced unexpected battery failure, fires, or fuel system problems linked to an allegedly defective battery may qualify.

Parents of children diagnosed with autism or ADHD who were fed commercial baby food from brands such as Gerber, Beech-Nut, Walmart (Parent's Choice), or Earth's Best Organic as infants — products found to contain elevated arsenic, lead, or cadmium — may qualify.

Consumers who purchased certain Quaker Oats, Cap'n Crunch, or other Quaker-brand food products recalled due to possible Salmonella contamination may qualify. A $6.75 million class settlement is currently open for eligible purchasers.

Parents who fed their infants Gerber or Beech-Nut baby food products and whose children were exposed to elevated levels of toxic heavy metals — arsenic, lead, cadmium, or mercury — found in those products may qualify, regardless of whether their child developed a specific diagnosis.

Consumers who purchased Costco Kirkland Signature rotisserie chicken and became ill from Salmonella, or who believe they were exposed to contaminated product without adequate disclosure, may qualify for this active food safety class action.