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.
West Elm Floor Lamp Recall Issued Due to Risk of Injury, Shocks April 24, 2013 Russell Maas Add Your CommentsHundreds of floor lamps sold at West Elm stores nationwide have been recalled from the market after at least 24 reports of the lamps failing, including three reports of the cords sparking. ย A West Elm Overarching floor lamp recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on April 23, due to problems with the lamp’s joint locking mechanism, which may fail and allow the lamp to collapse. This may create sparks from the cord and pose a potential risk of shocks or other injury for consumers.To date, 24 incident reports have been received by the manufacturer, including at least ten incidents where the West Elm floor lamp lamp fell and three incidents where the cords sparked. No injuries have been reported.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 COMPENSATIONThe recall affects Industrial Overarching floor lamps with a swiveling triple-jointed adjusting arm with model numbers 192799, 192856,465906, or 465922, which were manufactured between August 2012 and February 2013. The date of manufacture is located on a sticker under the base and in MM/YYYY format.The floor lamps measure 78 inches tall with a 12.5 inch high lamp shade and are 21 inches in diameter at the base with a antique bronze finish. The title “Industrial Overarching Floor Lamp” is displayed on the products packaging.The recalled overarching lamps were manufactured in China by Modern Home, of Guangdong, China and imported by West Elm, a branch of Williams-Sonoma Inc., of San Francisco. The lamps were sold exclusively in West Elm stores, catalogs, and online from December 2012 through February 2013 for about $380 with the lamp shade and $300 without the lamp shade.Consumers should immediately unplug the recalled lamp and return it to West Elm for a full refund or contact them at (855) 776-6953 or visit them online at www.westelm.com and navigate to the “Safety Recalls” link toward the bottom of the page for more information. 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: Electrocution, West Elm Image Credit: |More Lawsuit Stories SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation April 20, 2026 Lawsuits Over Cartiva Real-World Failure Rates Continue To Roll Into MDL April 20, 2026 Barton Pressure Cooker Lawsuit Claims Explosion Resulted in Third- and Fourth-Degree Burns April 20, 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 SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: today)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) Passenger in Uber Sexual Assault Trial Tells Jury She Feared Driver Knowing Her Address (Posted: 3 days ago)The second federal Uber sexual assault bellwether trial is underway in North Carolina, involving claims a woman was groped and had to flee from the driver.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITMDL Judge Appoints Lyft Sexual Assault Lawyers to Leadership Positions (03/30/2026)Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat (03/26/2026)Uber Settlements Reached To Resolve Certain Sexual Assault Lawsuits (03/18/2026) Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: 4 days ago)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. 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SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation April 20, 2026
Barton Pressure Cooker Lawsuit Claims Explosion Resulted in Third- and Fourth-Degree Burns April 20, 2026
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: today)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)
Passenger in Uber Sexual Assault Trial Tells Jury She Feared Driver Knowing Her Address (Posted: 3 days ago)The second federal Uber sexual assault bellwether trial is underway in North Carolina, involving claims a woman was groped and had to flee from the driver.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITMDL Judge Appoints Lyft Sexual Assault Lawyers to Leadership Positions (03/30/2026)Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat (03/26/2026)Uber Settlements Reached To Resolve Certain Sexual Assault Lawsuits (03/18/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: 4 days ago)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)