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.
Ford Battery Recall Affects 272,000 Bronco, Maverick Vehicles: NHTSANew recall comes after 19 vehicle owners reported continued battery problems following a previous repair that was supposed to fix the issue. January 24, 2025 Darian Hauf Add Your CommentsFederal highway safety officials have announced a recall of 272,817 Ford Bronco Sport and Maverick vehicles due to a potential defect with the battery, which could increase the risk of an auto accident.The U.S. National Highway Traffic Safety Administration (NHTSA) announced a Ford Bronco and Maverick recall on January 22, warning that manufacturing errors in the welding or strap features in certain vehiclesโ batteries could lead to sudden battery degradation and failure.The recall comes just nine months after Ford recalled more than 456,000 Bronco Sport and Maverick vehicles in April 2024, due to a battery malfunction in which the vehicles failed to detect a low battery charge, increasing the risk of sudden loss of electrical or drive power, which could lead to accidents.The previous recall was also part of an NHTSA investigation in November 2024, after Ford was fined $165 million for conducting an inaccurate recall that failed to include all of the affected vehicles and malfunction information. NHTSA investigated the prior recall after receiving at least 15 reports from vehicle owners who had received the repair but still experienced issues with power loss.Federal officials now warn that batteries in certain Ford Bronco Sport and Maverick vehicles may suddenly degrade while driving. This defect can prevent the vehicle from restarting after an auto stop/start event, cause it to stall at low speeds, or lead to a loss of battery-related accessories such as hazard lights, increasing the risk of accidents or injuries.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 COMPENSATIONFord first became aware of the current problem on September 24, 2024, after receiving an inquiry from the NHTSA Office of Defect Investigation (ODI) related to 19 vehicle owners alleging a loss of driving power after receiving a repair from the prior recall.On November 15, the ODI initiated a recall query to address the concern. Subsequently, from November through January 2025, the Low Voltage Power Supply team carried out an engineering evaluation of the returned defective batteries.The team determined that vehicles repaired under the previous recall were equipped with Enhanced Flooded Batteries supplied by Camel and Clarios. However, some of the Camel batteries have failed cast-on straps and internal welding issues. These defects can lead to open circuits and battery failure. Ford has not identified any problems with the batteries supplied by Clarios.According to the recall report (PDF), the software released as part of the earlier recall was unable to detect certain electrical signatures from failed batteries and did not disable the stop/start functionality quickly enough.On January 10, a field action was approved and a voluntary recall (PDF) was announced on January 22, impacting model year 2021 through 2023 Ford Bronco Sport and 2022 through 2023 Ford Maverick vehicles.Ford is not aware of any accidents, fires or injuries attributed to the defect.Customers will begin receiving notification letters on February 3, 2025, with instructions on how to schedule a free inspection and installation of a Ford Absorbed Glass Mat (AGM) 12V battery if needed.Any vehicle owners who have already had this repair performed at their own expense prior to receiving the Ford recall notification may be eligible for reimbursement.Fordโs number for this recall is 25S02. Customers may contact Ford customer service at 1-866-436-7332, or the companyโs contact for this recall, Dusty Gardner, via email at dusty.gardner@dot.gov.Owners with any additional questions may 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: Battery, Battery Recall, Ford, Ford Bronco, Ford Bronco Sport, Ford Maverick, NHTSA Image Credit: Shutterstock: ElninhoMore Lawsuit Stories Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026 Omnipod Class Action Lawsuit Filed Over Recalled Insulin Delivery System July 7, 2026 Lack of Safety Features Led to Roblox Child Exploitation, Lawsuit Claims July 7, 2026 0 Comments PhoneThis 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 Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026) Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration (Posted: yesterday)A Texas man’s lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026) Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (Posted: 5 days ago)Federal warnings and enforcement actions involving Olympus and other reusable medical scopes have raised concerns that design flaws may allow bacteria to remain trapped after cleaning, leading to serious infections and product liability lawsuits.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026
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