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.
Recalled Airbags Searchable by Vehicle Identification Numbers (VIN) June 18, 2015 Russell Maas Add Your CommentsFederal regulators have created a database that allows car owners to specifically search for their vehicle identification number (VIN) to verify whether they may be impacted by the recent recalls for Takata airbag inflators, which may cause airbags to rupture and send deadly debris into the passenger compartment.ย The National Highway Traffic Safety Administration (NHTSA) announced this week thatย it has uploaded roughly 34 million vehicle identification numbers (VIN) into the agency’s recall search system, including vehicles impacted by massive Takata airbag recalls that have been issued in recent months by several different major automakers.Given the large number of recalls and changes to the size and scope of vehicles impacted, the effort is designed to help vehicle owners confirm whether their vehicle may have faulty airbag inflators and encourage them to schedule the necessary repairs.Learn More AboutAirbag Recall LawsuitsMillions of Vehicles Were Recalled in 2014 Due to Exploding Airbags That Caused Injuries and Deaths.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutAirbag Recall LawsuitsMillions of Vehicles Were Recalled in 2014 Due to Exploding Airbags That Caused Injuries and Deaths.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONA new webpage has been created specifically for the airbag recall, which can be reached by visiting Safecar.gov/RecallsSpotlight. In addition to the VINs being added to the database, the agency will also provide regular updates on the status of this and other high priority recalls.With roughly 34 million vehicles recalled by 11 separate automakers, the Takata airbag recall has proven to be the countryโs largest and most complicated recall in history. The airbags can overinflate, bursting and firing metal sharts into the vehicles’ passenger compartments, potentially injuring or killing occupants.The Japan based Takata part supplier has come under scrutiny for not supply replacement parts in a timely fashion to dealers and a portion of the vehicles that have been repaired are deemed inadequate by the NHTSA and may still pose rupturing hazards.On May 18, the U.S. Department of Transportation issued a Consent Order to TK Holding Inc. (Takata), which requires the company to be cooperative with the agency in all future actions involving the current recall investigation. The NHTSA also announced that it is attempting to take legal oversight of the recall in order to organize and prioritize the replacement of the defective airbags.U.S. Transportation Secretary Anthony Foxx said in a press release that the Consent Order is a major step forward for public safety and that the agency is taking proactive steps necessary to sure the defective inflators are replaced with safe ones in a timely manner.The NHTSA is acting swiftly to take over control of the Takata recalls, as more recall announcements from automakers are issued. Just this month, more than three million more vehicles were recalled by Mazda, Honda and Toyota Motor Corp. for rupturing driver and passenger Takata airbags.More than 100 injuries have been reported and at least seven deaths, five of which were recorded in the U.S. due to the rupturing Takata airbag inflators. The Takata inflators pose a serious risk of death or injury due to the internal metal components rupturing when the airbag explodes, projecting pieces of shrapnel through the bag at rapid speeds into the cab toward the driver and passengers. Reports from first responders have mistaken Takata airbag fatalities as homicides by stabbing and gunshot wounds.NHTSA officials say that their oversight of the recall and repair process will not only structure the repair process in both a timely and anticipated safer manner, but will also allow for the agency to track how many potentially rupturing airbags are still on U.S. roadways throughout the process.Takata Airbag Inflator LawsuitsA growing number of Takata airbag inflator lawsuits are being filed nationwide on behalf of individuals who suffered severe injuries from an exploding airbag. All involve similar allegations that design defects caused the airbags to overinflate and rupture.On February 5, the U.S. Judicial Panel on Multidistrict Litigation ordered all airbag lawsuits against Takata filed in federal courts nationwide to be consolidated under one judge for pretrial proceedings as part of a Takata airbag MDL.Complaints filed throughout the federal court system will be transferred to U.S. District Judge Federico Moreno in the Southern District of Florida to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings from different judges and to serve the convenience of the parties, witnesses and the courts.The decision initially only affects at least five class action lawsuits filed in three different federal districts. However, more than 67 other pending actions have been identified in about 20 different districts, which will also be transferred into the Takata airbag MDL, since they raise common allegations of fact and law. 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: Airbag, Airbag Recall, Auto Accident, Auto Recall, TakataMore Takata Airbag Lawsuit Stories Ford Fined $165M Over Inaccurate Recall That Was Conducted Too Slowly for Customer Safety November 21, 2024 Volkswagen Airbag Recall Impacts Nearly 115,000 Beetles and Passats November 11, 2024 BMW Recall Issued for Nearly 400K Vehicles with Airbags That May Explode July 16, 2024 0 Comments FacebookThis 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 Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine 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) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 5 days ago)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)
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