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.
Roundup Cancer Claim Goes Before Federal Jury, With Restrictions on Evidence in First Phase February 25, 2019 Austin Kirk Add Your CommentsJury selection is set to begin today in a California federal court, involving the first bellwether trial over claims that Roundup exposure causes non-Hodgkin’s lymphoma and other cancers.The trial will involve an unorthodox format, with the U.S. District Judge presiding over the litigation previously deciding to split the case into two separate phases, with the jury first considering whether the weedkiller caused the plaintiff’s cancer, before determining whether Monsanto should be held liable for withholding safety warnings and instructions from consumers.As a result, the scope of evidence that will be permitted in the first phase will be restricted, keeping out much of the inflammatory evidence that suggests Monsanto has known their weedkiller increases the risk of cancer for decades, yet continued to market the product as safe.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 COMPENSATIONIn a pretrial order (PDF) issued on February 24, the court denied Monsanto’s last attempt to dismiss a series of three federal bellwether claims, indicating that plaintiff’s specific causation experts may testify at trial that exposure to glyphosate contained in Roundup caused their diagnosis of non-Hodgkins lymphoma.As a result of the ruling, jury selection is expected to begin as scheduled today in San Francisco, involving a complaint (PDF) filed by Edward Hardeman, who claims that his 2015 diagnosis of large B-cell non-Hodgkins lymphoma was caused by Roundup used on his property to control poison oak and weeds since the 1980s.The trial will be closely watched by other plaintiffs, lawyers and investors, as a sign for how juries may respond to similar evidence that may be presented in more than 10,000 other Roundup cancer claims pending in courts nationwide.Each of the cases involve similar allegations that glyphosate and other ingredients contained in the widely used herbicide resulted in a diagnosis of non-Hodgkins lymphoma, which may have been avoided if Monsanto had provided adequate warnings and safety instructions for consumers.The Haderman claim will be the second to go before a U.S. jury, after a California state-court lawsuit filed by a former school groundskeeper diagnosed with non-Hodgkins lymphoma went to trial over the summer. After initially resulting in a jury award of $289 million, including $39 million in compensatory damages and $250 million in punitive damages designed to punish Monsanto for recklessly disregarding the safety of consumers, the trial judge issued a reduced judgment of $78.5 million in that case, which was granted an expedited trial date in California state court since the plaintiff is dying.Trial Split Into Two PhasesThe federal court’s rare decision to split the next bellwether Roundup trial into multiple phases was aggressively opposed by plaintiffs, who argued that it would confuse the jury and limit the usefulness of any verdict in the claim.While evidence presented during this first phase will be restricted, last month the judge presiding over the litigation rejected a request by Monsanto to exclude all evidence that the manufacturer tried to manipulate the science to make the weed killer appear safe, calling evidence and internal documents indicating the company had manipulated allegedly independent studies and regulators โsuper relevantโ to the plaintiffโs claims that glyphosate causes non-Hodgkins lymphoma.In another pretrial order (PDF) issued on February 18, the court did grant a number of motions in Limine filed by Monsanto, which will exclude a monograph by the International Agency for Research on Cancer (IARC), from the first phase of the trial.The IARC, which is part of the World Health Organization, determined in March 2015 that glyphosate was a probable human carcinogen, linking it to an increased risk of non-Hodgkinโs lymphoma, and sparking much of the current litigation. The ruling bars the monograph by the respected cancer organization, describing it as a review of other studies, and not evidence itself. However, expert witnesses are still allowed to discuss and describe to the jury the IARCโs classification and meta-analysis.The Judge also granted a request by Monsanto to exclude evidence that the company had ghostwritten some studies from the first phase of the trial, but indicated that evidence will be allowed in the second phase, if the jury finds that the plaintiff met the necessary burden of proof in the first phase.Following this case and at least two other federal bellwether claims scheduled for trial this year, as well as a number of other state court trial dates set throughout 2019, if Monsanto fails to negotiateย Roundup settlementsย or otherwise resolve the litigation, the company is likely to face an increasing number of individual trial dates in courts nationwide in the coming years. Tags: Cancer, Glyphosate, Herbicide, Monsanto, Non-Hodgkins Lymphoma, Roundup, Weed Killer Image Credit: |More Roundup Lawsuit Stories Judge Grants Preliminary Approval to Roundup Lawsuit Settlement Plan March 5, 2026 $7.25B Roundup Class Settlement Proposed To Resolve Non-Hodgkin’s Lymphoma Lawsuits February 18, 2026 Roundup Settlement Program Remains Option With Supreme Court Review Pending: MDL Judge February 9, 2026 0 Comments URLThis 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 Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: yesterday)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: 2 days ago)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 3 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
$7.25B Roundup Class Settlement Proposed To Resolve Non-Hodgkin’s Lymphoma Lawsuits February 18, 2026
Roundup Settlement Program Remains Option With Supreme Court Review Pending: MDL Judge February 9, 2026
Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: yesterday)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)
Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: 2 days ago)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026)
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 3 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)