Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Safety of Monsanto’s Roundup Questioned During Four-Day EPA Safety Hearing December 21, 2016 Irvin Jackson Add Your CommentsA panel of scientific advisers are conducting a safety review to evaluate the potential side effects of exposure to Roundup, Monsanto’s popular weed killer, raising questions about federal regulators’ recent claims that the active ingredient glyphosate is not likely to cause cancer.ย The scientific advisory panel met last week for four days at the behest of the U.S. Environmental Protection Agency (EPA), to review the scientific evidence for and against a link between glyphosate and cancer, specifically non-Hodgkin’s lymphoma. The hearings were contentious, with claims of industry bias on behalf of the EPA, and questions about the exclusion of one proposed panel member.Concerns over the risk of non-Hodgkin’s lymphoma from Roundup exposure gained widespread media attention last year, after the World Health Organizationโs International Agency for Research on Cancer (IARC) determined thatย glyphosate is a probable human carcinogen.ROUNDUP LAWSUITSWere you or a loved one exposed to RoundUp?Exposure to RoundUp has been linked to an increased risk of developing Non-Hodgkin’s Lymphoma and other cancers. RoundUp cancer lawsuits are being actively investigated.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONROUNDUP LAWSUITSWere you or a loved one exposed to RoundUp?Exposure to RoundUp has been linked to an increased risk of developing Non-Hodgkin’s Lymphoma and other cancers. RoundUp cancer lawsuits are being actively investigated.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe warning sparked world-wide debate about the widespread use of Roundup and other glyphosate-based weedkillers, raising questions about why Monsanto failed to warn farmers, landscapers, gardeners and other consumers about the potential Roundup risks.Before the hearing, the EPA submitted an evaluation of glyphosate (PDF) indicating that it is not likely carcinogenic. However, some of the 15 scientists on the panel raised questions about the agency’s methodologies, questioning why some evidence was included and others excluded.The IARC’s findings were based off of only peer-reviewed, independent research on glyphosate and its potential cancer effects. However, the EPA excluded some of those studies and also relied on studies conducted by industry interests and studies which were never published or peer-reviewed, the panel and some speakers noted.Some said that it appeared the EPA violated its own guidelines in its selection of evidence, by excluding a number of peer-reviewed studies which found a statistically significant link between glyphosate and non-Hodgkin’s lymphoma, which EPA officials defended by claiming they exercised “professional judgment.”In addition, it appears the EPA kicked one member, Dr. Peter Infante, off of the panel at the request of the industry trade group CropLife America. The EPA said his removal from the panel was voluntary, however, Infante, who has worked for the Occupational Safety and Health Administration and the National Institute for Occupational Safety and Health, showed up as a speaker, and has said his removal was not voluntary as the EPA claims.Infante has been critical of industry-sponsored studies in the past, and has testified in some cases as an epidemiological expert on pesticide side effects. CropLife claimed that he is biased against industry and should not be part of the panel.In a letter sent on December 12, the Center for Food Safety claimed that Infante’s removal from the Science Advisory Panel (SAP) violates Congressional guidelines on how advisory groups are formed.“Dr. Infante is a highly regarded epidemiologist with a long record of public service, including a stint on an EPA advisory board, who possesses the technical expertise to assess glyphosate’s carcinogenic potential,” the letter states. “The EPA dismissed Dr. Infante only after duly appointing him to the SAP, in response to pressure from a special interest, the pesticide industry lobby group CropLife, in violation of the Federal Advisory Committee Act.”The panel has 90 days to pour over the testimony, literature and evidence presented during the hearing, after which it will submit recommendations to the EPA. Those recommendations are non-binding, but usually have significant influence on the agency’s final decisions.Roundup LitigationMonsanto now faces a growing number of Roundup cancer lawsuits filed throughout the United States, typically involving individuals diagnosed with a form of non-Hodgkinโs lymphoma following heavy exposure to the herbicide as a farm or agricultural worker.The complaints allege that the manufacturer recklessly promoted Roundup and pushed greater and greater use of the chemical, without disclosing the potential health risks.A recent U.S. Geological Survey on glyphosate usage nationwide foundย that an estimated 2.6 billion pounds of the herbicide has been sprayed on Americaโs agricultural land over the two decades since the mid-1990s, when Monsanto introduced โRoundup Readyโ crops that are designed to survive being sprayed with glyphosate, killing the weeds but not the crops.The lawsuits over Roundup allege that plaintiffs may have avoided a diagnosis of non-Hodgkinโs lymphoma or other cancers if they had been warned about the Roundup risks for farmers, landscapers and others in the agricultural industry, as safety precautions could have been taken or other products could have been used to control the growth of weeds. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Cancer, Glyphosate, Herbicide, Monsanto, Non-Hodgkins Lymphoma, Roundup, Weed KillerMore Roundup Lawsuit Stories Roundup Class Action Lawsuit Linked to $7.2B NHL Settlement Transferred to Federal MDL June 2, 2026 MDL Judge Urged To Block $7.25B Roundup Non-Hodgkinโs Lymphoma Settlement April 28, 2026 Judge Grants Preliminary Approval to Roundup Lawsuit Settlement Plan March 5, 2026 0 Comments FacebookThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 3 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 4 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 5 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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