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.
GM Ignition Recall Expanded Again, Previous Settlements Questioned March 31, 2014 Irvin Jackson Add Your CommentsGeneral Motors is recalling another 824,000 vehicles in the United States, bringing the total number of vehicles impacted the ignition switch problems to nearly 2.6 million. The recall expansion comes just days before CEO Mary Barra is set to go before Congress to explain why the company took more than a decade to address the problem. ย The recall expansion was announced on March 28, indicating that GM will replace the ignition switch in all model years of the Chevrolet Cobalt, HHR, Pontiac G5, Solstice and Saturn Ion and Sky vehicles.GM indicates that it has expanded the recall because dealers may have unknowingly replaced ignition switches with just another faulty switch before information about the problems was released.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 COMPENSATIONIn February, General Motors first announced that problems with ignition switches in certain vehicles may cause the cars to shut off unexpectedly when heavy keys are used or the ignition is jarred, such as in an auto accident.If the ignition switch shuts off then the air bags are disabled and will not deploy in an accident. The auto maker has acknowledged that at least 13 deaths may be linked to the problem, but outside analysts say that number could be in the hundreds.The expansion adds 824,000 vehicles to the recall in the U.S., and 971,000 worldwide, raising the total number of vehicles affected to 2.59 million.GM called the step to expand the recall to additional vehicles “extraordinary” and said the move is meant to ensure that all of the defective switches are taken off the market. The company estimates that about 95,000 faulty switches were sold to dealers and aftermarket wholesalers, who used about 90,000 of them to repair older vehicles before the recall was announced.“We are taking no chances with safety,” Barra said in the press release. “Trying to locate several thousand switches in a population of 2.2 million vehicles and distributed to thousands of retailers isn’t practical. Out of an abundance of caution, we are recalling the rest of the model years.”Barra said the goal is to make sure that new switches are installed in all vehicles and to provide peace of mind to GM customers.The company says the switches may have been used in repairs on 2008-2010 model year Chevrolet Cobalts, 2008-2011 Chevrolet HHRs, 2008-2010 Pontiac Solstice vehicles, 2008-2010 Pontiac G5 vehicles, and 2008-2010 Saturn Sky vehicles.The company says owners they suspect may have gotten one of the replacement switches will receive a letter the week of April 21. The ignition switches will be replaced free of charge as parts become available, and those who have already gotten their ignition switch replaced will be eligible for reimbursement.GM ControversyThe decision to expand the recall comes as the company continues to take heat over the problem with the ignition switches. GM has admitted that it knew about the problem since at least 2001, and failed to take actions to remove the vehicles from the road.The company now faces a growing number of ignition switch recall lawsuits, including wrongful death claims and class action lawsuits by owners. In addition, given the new information, two families who reached wrongful death settlements with the company over fatalities related to the ignition switch problem before the recall was announced are now looking for a way to get those settlements overturned.The families say they were unaware that GM knew of the problems before the accidents occurred and that the settlements were reached under false pretenses. Both families are investigating their options on overturning the settlements, which may be legally difficult.GM also faces two congressional investigations, and the Department of Justice is looking into the possibility of criminal charges. Barra is scheduled to testify before the U.S. House of Representatives and the U.S. Senate on April 1 and April 2, respectively.The House Energy and Commerce Committee issued a briefing and timeline of events (PDF) on March 30 ahead of the hearing. The briefing highlights the results of its investigation into the recall, revealing that in February 2002, GM parts supplier Delphi warned GM that the sample testing of the ignition switch torque was below the original specifications. 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, Auto Recall, Chevrolet Cobalt, Chevrolet HHR, Class Action Lawsuit, Congress, General Motors, Pontiac G5, Pontiac Solstice, Saturn Ion, Saturn Sky, Wrongful Death Image Credit: |More Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 0 Comments LinkedInThis 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)
Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)
Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)