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.
California Judge Rules That Fluoride in Water Decreases Children’s IQEPA is now required to review acceptable levels of fluoride in drinking water, due to concerns about neurological side effects for children. September 30, 2024 Michael Adams Add Your CommentsAfter federal regulators rejected a request to review the safe levels of fluoride in U.S. drinking water, a California judge has ordered the government to take action, due to concerns that side effects of fluoride could lower children’s IQ.The decision (PDF) came in response to a lawsuit filed against the U.S. Environmental Protection Agency (EPA) by Food & Water Watch Inc., Fluoride Action Network and Moms Against Fluoridation, after the EPA refused to act on a petition filed by the groups, which challenged the agency’s decision to allow fluoride levels in U.S. drinking water to remain the same.The lawsuit was filed in the U.S. District Court for the Northern District of California in accordance with the Toxic Substances Control Act (TSCA), which was amended in 2016, allowing citizens to petition the EPA to investigate substances they believe pose an “unreasonable risk” to human health.According to TSCA, individuals and organizations can also request a judicial review of any EPA denial of their petition. The court can then independently assess if the substance in question is dangerous, even if the EPA previously deemed it safe.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know About…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAcceptable Levels of Fluoride Could Present Danger to ChildrenFluoride is a naturally occurring mineral that has been added to drinking water, foods and dental products worldwide for decades, due to its ability to help prevent tooth decay and strengthen bones.However, in 2006, the National Research Council determined that fluoride can also interfere with human body and brain functions, especially in children, potentially lowering their IQ.Following these findings, U.S. recommended levels of fluoride were lowered, with the acceptable amount in tap water set at 0.7 mg/L in 2015. The U.S. Food and Drug Administration (FDA) applied the same maximum level of fluoride to bottled water in 2022, to mitigate health risks, while continuing to provide dental benefits.Since that time, an increasing amount of scientific evidence has been presented linking fluoride to adverse neurological conditions, including exposure during pregnancy increasing risks of autism and ADHD in unborn children.As a result, Food & Water Watch Inc., Fluoride Action Network and Moms Against Fluoridation filed a petition with the EPA in November 2016, asking the agency to reconsider acceptable levels of fluoride in drinking water.However, the EPA subsequently denied the petition on February 17, 2017, maintaining that the negative findings in the research presented concerning fluoride had an insufficient basis in science.In accordance with the TSCA, the organizations then chose to file a complaint in federal court, asking the court to force the EPA to take some form of regulatory action against the dangers presented by fluoride in drinking water.EPA Must Reconsider Acceptable Fluoride Levels in Drinking WaterOn September 24, Judge Edward M. Chen issued a Findings of Fact and Conclusions of Law, ruling that there is ample scientific evidence that fluoride presents a risk of unreasonable injury to humans.The court determined that water fluoridation at the standard level of 0.7 mg/L presents an unreasonable risk of reduced IQ in children, and that the EPA itself agrees that some level of exposure to fluoride is dangerous.“There is little dispute in this suit as to whether fluoride poses a hazard to human health. Indeed, EPA’s own expert agrees that fluoride is hazardous at some level of exposure. And ample evidence establishes that a mother’s exposure to fluoride during pregnancy is associated with IQ decrements (reductions) in her offspring,” said Judge Chen in the recent decision.Judge Chen also stated that under the TSCA, the substance being decided upon does not have to be found hazardous at the minimum level of exposure for the EPA to be required to reconsider acceptable levels, only that there is uncertainty as to what level of exposure is harmful.In addition, after a judicial finding of an unreasonable risk, the EPA is legally compelled to respond appropriately.While the court did not specify what the final rule must entail, Judge Chen has issued a binding order that requires the EPA to take regulatory action to address the risk posed by fluoride in drinking water, which could include revising permissible fluoride levels, among other potential regulatory responses, so as to mitigate the risk to human health, particularly to children. Written by: Michael AdamsSenior Editor & JournalistMichael Adams is a senior editor and legal journalist at AboutLawsuits.com with over 20 years of experience covering financial, legal, and consumer protection issues. He previously held editorial leadership roles at Forbes Advisor and contributes original reporting on class actions, cybersecurity litigation, and emerging lawsuits impacting consumers. Tags: Childrens Health, Drinking Water, EPA, Fluoride, IQ, TSCAMore Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 0 Comments CommentsThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: today)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addict’s ‘Self-Exclusion’ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: yesterday)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 2 days ago)A Florida woman’s lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026
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Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: yesterday)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
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