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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Saturn VUE Recall Issued Due to Risk of Key Coming Out While On August 18, 2014 Irvin Jackson Add Your CommentsGeneral Motors (GM) is recalling more than 200,000 Saturn VUE vehicles, due to problems with the ignition that may allow the key to come out while the vehicle is still running.ย The Saturn VUE recall was announced on August 8, impacting vehicles from the 2002 through 2004 model year.According to GM, the ignition key can be removed when the vehicle is not in the off position, which may have caused at least two auto accidents and one injury.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 is the latest in a series of more than 60 GM recalls issued this year, which have affected about 30 million vehicles, nearly half of which involved various ignition switch problems.The companyโs problems began in the early part of the year, when the NHTSAโs investigation into 13 deaths of drivers whose air bags did not deploy was concluded to be from faulty ignition switches in roughly 2.6 million GM vehicles.GM had reportedly known about the ignition switch issue for more than a decade before issuing theย ignition switch recall, which prompted a $35 million fine from the NHTA for delaying a recall. In addition to the government fines and penalties, the company has established aย victims compensation fundย created for owners and passengers who were injured or killed in some of those vehicles.The Saturn VUE recall affects 202,115 vehicles, with owners being advised to make sure the vehicle is in “Park” or, in the case of a manual transmission, to put the vehicle into reverse gear and set the parking brake before removing the key and getting out.The recall was the largest of several announced on August 8. The second-largest affects 48,059 2013 Cadillac ATS four-door sedans and 2013 Buick Encore vehicles that may have seatbelt problems which can lead to the seatbelts not properly preventing movement during an accident. The company discovered the problem during testing and has issued a stop sale order. There are no reports of crashes or injuries associated with the defective seatbelts.Another 14,940 Chevrolet Impala LT and LTZ model sedans from the 2014 and 2015 model years reportedly have defective console storage compartment latches, which may cause them to spring open during a rear collision. GM also recalled 1,968 Chevrolet Aveo vehicles from 2009-2010, and Pontiac G3 vehicles from 2009, due to brake fluid problems that could affect braking performance, and 1,919 Chevrolet Spark vehicles from 2014 for left and right lower control arm bolts that may not be properly tightened.Ignition Switch LawsuitsA growing number of GM ignition switch lawsuits are being filed by owners, investors and those who have been injured in accidents, despite the company’s victim compensation fund. The lawsuits include claims by those who say they were economically damaged by the companyโs actions, and those who were injured or lost loved ones in recalled vehicles not included in the compensation fund.In early June, the U.S. Judicial Panel on Multidistrict Litigation issued an orderย consolidating all economic lawsuits against GMย under U.S. District Judge Jesse M. Furman in federal court in New York for pretrial proceedings. The next scheduled conference is set for August 11, at which time Furman may select attorneys for leadership roles in the litigation.Late last month, a product liability lawsuit was filed on behalf of families ofย 29 people who died in accidents linked to ignition switch defects, as well as for more than 600 people who were injured. All of the claims come from among the 17 million vehicles that GM has recalled for ignition switch problems, but for which it has refused to offer compensation. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Auto Accident, General Motors (GM), Ignition Switch, SeatbeltMore GM Ignition Recall Lawsuit Stories Auto Safety Oversight Lacking At NHTSA, According to Audit February 29, 2016 Second GM Recall Lawsuit Headed to Trial March 14, After First Bellwether Dismissed Amid Fraud January 29, 2016 GM Bellwether Trial Begins Over Claims Airbag Did Not Deploy Due to Ignition Switch January 11, 2016 0 Comments CompanyThis 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: yesterday)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
Second GM Recall Lawsuit Headed to Trial March 14, After First Bellwether Dismissed Amid Fraud January 29, 2016
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: yesterday)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)