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 Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
Hyundai, Kia Electric Car Recalls Affect More Than 200,000 Genesis, Ioniq and EV6 VehiclesManufacturers are expanding a previous electric vehicle recall, after the original repair solution did not appear to work. November 27, 2024 Darian Hauf Add Your CommentsFederal highway safety officials have announced electric car recalls impacting Kia EV6, Hyundai Genesis and Hyundai Ioniq vehicles from the 2022 to 2025 model years, which may contain damaged charging units that could cause a sudden loss of power, potentially increasing the risk of an auto accident.Two separate notices were posted by the U.S. National Highway Traffic Safety Administration (NHTSA) on November 21, including a Kia recall impacting 62,872 EV6 electric vehicles and a Hyundai recall impacting 145,235 Genesis and Ioniq electric cars, warning that certain vehicles equipped with an Integrated Charging Control Unit (ICCU) may experience damage that prevents the 12-volt battery from charging, potentially resulting in a loss of driving power.The ICCU is responsible for charging the vehicle’s auxiliary battery and powering low-voltage accessory equipment. However, under certain conditions, the ICCU in the affected vehicles may blow a fuse, preventing it from charging. If this occurs, it may lead to the battery becoming fully depleted, at which point the car could lose all driving power.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 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 COMPENSATIONThe following Hyundai and Kia vehicles are impacted by the electric car recall:2023-2024 Hyundai Genesis G80 EV2023-2025 Hyundai Genesis GV602023-2025 Hyundai Genesis GV70 EV2022-2024 Hyundai Ioniq 52023-2025 Hyundai Ioniq 62022-2024 Kia EV6The manufacturers advise drivers to look for warning indications that may signal an impending loss of motive power, such as illuminations on the dashboard, audible chimes, warning messages or noticeable decreases in the vehicle’s power or speed.Customers may notice that when their car’s computer systems detect the fault, the vehicle will enter a “fail-safe” driving mode, where airbags, braking and powered steering remain operational.The NHTSA reports that Kia and Hyundai have not identified any accidents or injuries related to the defect.Previous Hyundai and Kia RecallsThis new recall follows ones made in March 2024, when Kia recalled 48,232 EV6 vehicles and Hyundai recalled 98,878 Ioniq and Genesis vehicles for the same issue.Hyundai Motor Company (HMC) first became aware of issues concerning certain Genesis and Ioniq vehicles in October 2022, when warranty claims identified heat damage to ICCU transistors in the vehicles.HMC was then notified in April 2023 that some Genesis and Ioniq vehicles were reporting a loss of driving power. In May 2023, the ICCU was identified as the cause. After further investigation and testing, the manufacturer conducted a safety recall in March 2024 with instructions to obtain updated ICCU software.Kia North America (Kia NA) was first notified about issues regarding the ICCU in certain EV6 vehicles by the company’s Safety Office in May 2023. The company then conducted a voluntary service campaign for the affected vehicles after receiving reports of driving power losses without warnings.After further investigation and 34 reports of a loss of driving power, Kia NA conducted a recall of all 2022-2024 Kia EV6 vehicles in March 2024 with instructions to obtain updated ICCU software.New Kia and Hyundai RecallsDespite the previous recall, Kia has received an additional 88 reports, and Hyundai has received another 57 reports of similar issues between March 25 and November 5, 2024, including vehicles that had the previous recall fix performed on them.This has led the manufacturers to conduct the current recall for all affected vehicles, including those involved in the previous recall.Notification letters will be sent to Kia owners on December 13, and Hyundai owners on January 17, with instructions on how to schedule a free ICCU software update at their local dealer.The software associated with these recalls applies specifically to the LDL output voltage “soft start” that prevents overvoltage at the start and end of the battery charging cycle.Any vehicle owners who have already had this service performed at their own expense may be eligible for reimbursement, in accordance with each manufacturer’s reimbursement plan.Kia’s number for this recall is SC327. Customers can contact Kia customer service at 1-800-333-4542.Hyundai’s numbers for this recall are 272 (Hyundai) and 025G (Genesis). Customers can contact Hyundai customer service at 1-855-371-9460 or Genesis customer service at 1-844-340-9741.Both companies’ contact for this recall is Emily C. Smith, who can be reached via email at emily.c.smith@dot.gov.Owners with any additional questions can also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov. Written by: Darian HaufConsumer Safety & Recall News WriterDarian Hauf is a consumer safety writer at AboutLawsuits.com, where she covers product recalls, public health alerts, and regulatory updates from agencies like the FDA and CPSC. She contributes research and reporting support on emerging safety concerns affecting households and consumers nationwide. Tags: Electric Car, Electric Car Recall, Electric Vehicle, Hyundai, Hyundai Genesis, Hyundai Ioniq, Kia, Kia EV6 Image Credit: Shutterstock: Kirill GorshkovMore Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 0 Comments X/TwitterThis 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: 2 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) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 3 days ago)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: 4 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)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 2 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)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 3 days ago)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: 4 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)