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.
Gabapentin Dementia Lawsuit Gabapentin dementia lawsuits are being investigated against Pfizer and other drug manufacturers following studies linking the widely prescribed medication to an increased risk of dementia, Alzheimer's disease and mild cognitive impairment. Learn about the allegations, recent research, lawsuit updates and potential settlement compensation.
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
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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
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.
E-Cigarette Makers Face Looming Deadline To Obtain FDA Approval For Vaping Products August 18, 2020 Russell Maas Add Your CommentsA deadline is fast-approaching for manufacturers of e-cigarettes to obtain FDA approval for their products, leaving a number of companies scrambling to keep their vaping products on the market, according to a new report by Convenience Store News.In August 2016, the U.S. Food and Drug Administration (FDA) published their final e-cigarette guidance in the Federal Register, claiming regulatory responsibility of all Electronic Nicotine Delivery Systems (ENDS), which includes e-cigarettes, vaping products, and all liquids used with the devices.The guidance classified ENDS devices as tobacco products, allowing the FDA to take control of an unregulated market, which gained national attention due to a series of problems including exploding lithium ion batteries and the illegal marketing of tobacco products targeting teens and adolescents.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 AboutโฆSpinal 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 COMPENSATIONAs a result of the action, the FDA mandated that all new nicotine based products go through premarket tobacco product applications (PMTAs) pursuant to the Tobacco Control Act that was passed in February 2007.Manufacturers that fail to submit their PMTAs by the deadline will be prohibited from selling their products on the U.S. market, and be required to remove all of their vaping products from the market before this deadline. Manufacturers and stores that fail to comply with these standards will be subject to penalties assigned by the FDA.In July 2019, a U.S. District Court in Maryland ordered that applications for deemed tobacco products, such as e-cigarettes, cigars, pipe tobacco, and hookah tobacco, that were on the market as of August 8, 2016, must be submitted to FDA no later than May 12, 2020. However, due to the ongoing COVID-19 pandemic, the deadline was extended in April through September 9, 2020.By the deadline, manufacturers are required to submit for approval on how they intend to market their products in a way that discourages teen and underage use. The guidance also calls for manufacturers to provide details on how they intend to prevent lithium ion batteries used in e-cigarettes from exploding.To date, several major ENDS manufactures have submitted their PMTAs, some for the second or third times, according to the CSNews.com report on August 17.One of the largest brand names submitting for approval is JUUL Systems, which currently faces more than 600 lawsuits, some of which claiming the manufacturer mined the middle and high school environments with easily concealable USB-like vaping products containing a highly addictive nicotine salt formulation in an effort to make life-long customers out of children.JUUL has reportedly submitted detailed scientific data from more than 110 studies that includes more than 125,000 pages evaluating the product’s impact on current users and those exposed to secondhand exposure. The research submitted also includes data and strategies oriented towards preventing youth and teenager first use.Among other major retailers that have submitted PMTAs to the FDA are Reynolds American Inc., Fontem US LLC, E-Alternative Solutions, 511 Solutions LLC and Altria Group Inc.The FDA announced it will evaluate the data and scientific information provided in the applications to determine whether the products are appropriate for the protection of public health. If approved the FDA will issue a Marketing Order Letter to authorize the continued marketing and sale.E-Cigarette ConcernsThe aggressive actions taken by the FDA over the last several years are in response to the rapid growth in e-cigarette use, with ENDS becoming the most popular form of tobacco, specifically among teens.Recent data has shown youth nicotine use jumping 78% from 2017 to 2018, according to the FDA. In 2011, when the FDA first said it would regulate e-cigarettes, only 1.5 percent of teens vaped, but now more than one-third of teens use e-cigarettes as they have become increasingly popular among all age ranges.The Centers for Disease Control and Prevention (CDC) found nearly 14% of middle school students, and 38% of high school students reported having used e-cigarettes. Among use in the last 30 days from when the survey was taken, five percent of middle schoolers and 16% of high school students reported having used vaping devices. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: E-Cigarettes, Electronic Cigarettes, Juul, VapingMore Lawsuit Stories Neurontin Dementia Lawsuit Alleges Gabapentin Caused Early-Onset Memory Loss November 10, 2026 Cartiva Lawsuits Over Toe Implant Problems Moving Forward in Federal MDL November 10, 2026 Argon Option Elite IVC Filter Lawsuit Alleges Device Fractured, Leaving Metal Fragment Inside Woman November 10, 2026 0 Comments EmailThis 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 Neurontin Dementia Lawsuit Alleges Gabapentin Caused Early-Onset Memory Loss (Posted: today)A womanโs lawsuit claims prolonged use of gabapentin to treat nerve pain resulted in significant memory problems, cognitive decline and early-onset dementia.MORE ABOUT: GABAPENTIN DEMENTIA LAWSUIT FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk (Posted: yesterday)Federal regulators are requiring all GLP-1 medications to carry new label warnings indicating the side effects could put patients at risk of sudden and permanent vision loss.MORE ABOUT: OZEMPIC LAWSUITOzempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (10/30/2026)GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026) Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL (Posted: yesterday)Individuals involved in Boston Scientific SCS implant lawsuits have submitted a Master Complaint that would help streamline future filing.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (11/02/2026)Abbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)
Argon Option Elite IVC Filter Lawsuit Alleges Device Fractured, Leaving Metal Fragment Inside Woman November 10, 2026
Neurontin Dementia Lawsuit Alleges Gabapentin Caused Early-Onset Memory Loss (Posted: today)A womanโs lawsuit claims prolonged use of gabapentin to treat nerve pain resulted in significant memory problems, cognitive decline and early-onset dementia.MORE ABOUT: GABAPENTIN DEMENTIA LAWSUIT
FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk (Posted: yesterday)Federal regulators are requiring all GLP-1 medications to carry new label warnings indicating the side effects could put patients at risk of sudden and permanent vision loss.MORE ABOUT: OZEMPIC LAWSUITOzempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (10/30/2026)GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)
Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL (Posted: yesterday)Individuals involved in Boston Scientific SCS implant lawsuits have submitted a Master Complaint that would help streamline future filing.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (11/02/2026)Abbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)