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.
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
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.
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.
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.
Nissan Rogue Recall Issued Over Shift Selector Problems December 15, 2015 Russell Maas Add Your CommentsMore than 30,000 Nissan sport utility vehicles have been recalled, after the auto maker recognized the potential for the vehicleโs shifter to be move out of the โparkโ position without depressing the brake pedal, posing a potential rollaway risk and crash hazard.ย The Nissan Rouge recall (PDF) was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) on December 11, after routine testing at the companyโs Tennessee plant discovered design defects in the shifter assembly, which may allow the shifter to move out of the selected gear without depressing the brake.Nissan of North America reported to the NHTSA that during routine inspections at the Smyrna, Tennessee plant, certain model year 2015 Nissan Rogue vehicles exhibited transmission shift selector knob assembly issues. Upon further investigation, Nissan found that the shift selector knob and the shifter rod were causing uneven spring pressure. This defect, and an uneven clearance between the two components, could allow the shifter lever to change position without depressing the brake pedal.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 COMPENSATIONTo date, Nissan has back checked warranty claims and consumer reports, and has not identified any crashes or injuries related to the defect. However, as a result of the identified defect, the Rogue vehicles do not comply with the Federal Motor Vehicle Safety Standard 114, “Theft Protection and Rollaway Preventionโ, warranting the recall.Rollaway hazards can be extremely dangerous to drivers, occupants and bystanders. The NHTSA has reported in past recall incidents where children have entered vehicles and accidentally bumped the shifters without depressing the brake, resulting in rollaway and collision incidents, resulting in injuries, property damage, and even fatalities.Included in the recall are an estimated 33,880 Nissan Rogue vehicles from the 2015 model year, which were manufactured by Nissan North America, Inc. from February 10, 2015 through May 13, 2015. Nissanโs investigation identified that the manufacturing defect occurred as a direct result of the particular plants operations and no other vehicles are impacted by the recall.The NHTSA reported that Nissan will begin notifying owners and dealers of the defect and plans to have registered dealers inspect and replace the shift selector knob, as necessary, free of charge. The recall is anticipated to begin sometime in December 2015. Customers with further questions may contact Nissan customer service at 1-800-647-7261. 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: Auto Accident, Auto Recall, Nissan, Nissan Recall Image Credit: <a href="http://www.shutterstock.com/gallery-365671p1.html?cr=00&pl=edit-00">FotograFFF</a> / <a href="http://www.shutterstock.com/editorial?cr=00&pl=edit-00">Shutterstock.com</a>More Lawsuit Stories Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 September 14, 2026 Colsen Tabletop Fire Pit Lawsuit Alleges Defective Design Caused Flame Jetting Burn Injuries September 14, 2026 Roblox Arbitration Clause Opposed by U.S. Senators in Child Sexual Assault Lawsuit Appeal September 14, 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 Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (Posted: today)Attorneys will meet tomorrow for a final pretrial conference ahead of the third Bard PowerPort lawsuit bellwether trial.MORE ABOUT: BARD POWERPORT LAWSUITJury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026) Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: 4 days ago)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 5 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
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