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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Honda Minivan Recall For Nearly 250K Odyssey Vehicles Due To Fire Risk February 12, 2020 Russell Maas Add Your Comments A wiring problem in more than 240,000 Honda Odyssey minivans may cause a short circuit, resulting in a vehicles from the 2018 to 2020 model years. The Honda minivan recall was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) on February 11, after it was discovered that the wire harness for the third row seating may become pinched between the frame and rear trim panel, possibly damaging and exposing the wires. According to the manufacturer, the vehicles contain a third row seat accessory power outlet with wires which could become pinched, causing an electrical short. Officials warn that if this short circuit occurs, the wires could smolder and catch the interior on the vehicle on fire. Do You Know about… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Honda first became aware of the issue in August 2018, after receiving a report of a fire from a vehicle owner, but investigators were unable to reclaim the vehicle for investigation. By December 2019, two more vehicle fires had been reported, and a comprehensive investigation determined the root cause of the fire was a damaged wiring harness under the third row seat that had become pinched. As of January 30, 2020, Honda has received three warranty claims, five field reports, three reports of fires, and no reports of injuries related to this issue. The recall affects certain 2018 through 2020 Odyssey minivans manufactured by American Honda Motor Company of Torrance, California from January 19, 2017 through August 13, 2019. They were distributed for sale throughout the U.S. to licensed dealers. Honda announced it will be sending recall notices to customers with instructions on how to schedule a free repair appointment with their local dealer, who will be instructed to inspect the third row seat accessory power outlet wire harness for damage, and replace as necessary. For harnesses without damage, dealers will apply protective tape and re-route the wiring harness to avoid pinching hazards. The recall is expected to begin on March 16, 2020. Customers with additional questions or concerns regarding the recall may contact Honda customer service at 1-888-234-2138 and reference the recall number T6U. Tags: Auto Recall, Honda Odyssey, Vehicle Fire More Lawsuit Stories Infusion Pump Recalls Affect More Than 300,000 CADD-Solis Portable Devices: FDA June 5, 2025 Lawsuit Claims Biozorb Implant Penetrated Skin, Causing Massive Infection June 4, 2025 Consumer Argues Food Manufacturers Concealed UPF Diabetes, Fatty Liver Disease Risks for Children June 4, 2025 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Lawsuit Claims Biozorb Implant Penetrated Skin, Causing Massive Infection (Posted: yesterday) A BioZorb lawsuit claims that the recalled implant’s defective design led to the device migrating through a woman’s flesh, causing a severe infection. MORE ABOUT: BIOZORB LAWSUITBreast Cancer Survivors File BioZorb Tissue Marker Lawsuit After Implant Fails (05/20/2025)BioZorb Implant Lawsuit Alleges Tissue Marker Caused Swelling, Fluid Buildup and Chronic Pain (05/14/2025)Four Women File BioZorb Lawsuit Over Breast Tissue Marker Failures and Injuries (05/05/2025) More Than 1,700 Bard PowerPort Lawsuits Now Filed in State and Federal Courts (Posted: 2 days ago) As the number of Bard PowerPort lawsuits brought over design defects associated with the port catheter system continues to mount, lawyers have agreed on the first bellwether case that should go before a jury. MORE ABOUT: BARD POWERPORT LAWSUIT6 Bard PowerPort Lawsuits Selected for Bellwether Trials in Federal MDL (05/19/2025)Court Indicates Bard PowerPort MDL Bellwether Lawsuits Should Include 3 Infection, 2 Thrombosis and 1 Fracture Case (05/06/2025)Lawyers Proposed 11 Bard Implantable Port Catheter Lawsuits as Bellwether Trial Candidates (04/30/2025) Impella Pump Class Action Lawsuit Alleges Defects Caused Perforated Left Ventricle, Wrongful Death (Posted: 3 days ago) A widow has filed an Impella heart pump class action lawsuit following the discovery that her husband’s death was likely linked to the implant piercing his heart. MORE ABOUT: IMPELLA HEART PUMP LAWSUITAbbott HeartMate Mobile Power Unit Recalled Over Sudden Power Loss Risks (04/28/2025)Staph Responsible for Most Heart Implant Infections, Study Finds (04/15/2025)Medtronic Recall Issued for Open Heart Surgery Device With Loose Materials That Could Injure Patients (04/02/2025)
Consumer Argues Food Manufacturers Concealed UPF Diabetes, Fatty Liver Disease Risks for Children June 4, 2025
Lawsuit Claims Biozorb Implant Penetrated Skin, Causing Massive Infection (Posted: yesterday) A BioZorb lawsuit claims that the recalled implant’s defective design led to the device migrating through a woman’s flesh, causing a severe infection. MORE ABOUT: BIOZORB LAWSUITBreast Cancer Survivors File BioZorb Tissue Marker Lawsuit After Implant Fails (05/20/2025)BioZorb Implant Lawsuit Alleges Tissue Marker Caused Swelling, Fluid Buildup and Chronic Pain (05/14/2025)Four Women File BioZorb Lawsuit Over Breast Tissue Marker Failures and Injuries (05/05/2025)
More Than 1,700 Bard PowerPort Lawsuits Now Filed in State and Federal Courts (Posted: 2 days ago) As the number of Bard PowerPort lawsuits brought over design defects associated with the port catheter system continues to mount, lawyers have agreed on the first bellwether case that should go before a jury. MORE ABOUT: BARD POWERPORT LAWSUIT6 Bard PowerPort Lawsuits Selected for Bellwether Trials in Federal MDL (05/19/2025)Court Indicates Bard PowerPort MDL Bellwether Lawsuits Should Include 3 Infection, 2 Thrombosis and 1 Fracture Case (05/06/2025)Lawyers Proposed 11 Bard Implantable Port Catheter Lawsuits as Bellwether Trial Candidates (04/30/2025)
Impella Pump Class Action Lawsuit Alleges Defects Caused Perforated Left Ventricle, Wrongful Death (Posted: 3 days ago) A widow has filed an Impella heart pump class action lawsuit following the discovery that her husband’s death was likely linked to the implant piercing his heart. MORE ABOUT: IMPELLA HEART PUMP LAWSUITAbbott HeartMate Mobile Power Unit Recalled Over Sudden Power Loss Risks (04/28/2025)Staph Responsible for Most Heart Implant Infections, Study Finds (04/15/2025)Medtronic Recall Issued for Open Heart Surgery Device With Loose Materials That Could Injure Patients (04/02/2025)