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.
Honda and Acura Recall Issued Over Brake Master Cylinder Failure, Accident RiskIf the brake master cylinder detaches, vehicles affected by the Honda and Acura recall may be unable to stop when the brakes are used. July 7, 2023 Katherine McDaniel Add Your CommentsAmerican Honda Motor, Co. has issued a recall impacting more than 124,000 Honda Civic, Passport, Ridgeline, Pilot and Acura MDX vehicles, which are equipped with brake master cylinders that may fail during normal operation of the vehicle, increasing the risk of an auto accident.The U.S. National Highway Traffic Safety Administration (NHTSA) announced the Honda and Acura recall on July 3, after the manufacturer confirmed a defect in the assembly of the brake master cylinders may cause the cylinder to separate from the booster assembly and subsequently fail.Officials warn that a brake master cylinder separation and failure event can occur without warning while the vehicle is moving, and can diminish or cause complete failure of the vehicleโs braking function, hindering the driverโs ability to stop the vehicle.The affected brake master cylinder is attached to the brake booster inside of the engine compartment firewall, and is an essential component which the entire brake system relies on in order to function properly. Once the brake pedal is activated, brake fluid is forced through the cylinder to build hydraulic pressure, which is then applied to pistons and forces friction against the wheel hubs to stop the vehicle.However, in the event the brake master cylinder separates from the brake booster assembly and fails, the braking system function will also fail and the vehicle will lose its ability to stop.Honda initially became aware of the issue in December 2020, after the automaker’s manufacturing facility found a nut missing from the tie rods of a vehicleโs brake booster assembly. While Honda states they promptly notified their part supplier to prevent further incidents, an investigation was later opened in December 2022, after the automaker received a report of a braking system failure in a 2021 Honda Pilot.The automaker determined that the issues stemmed from an improper assembly during the manufacturing of the braking system. According to the recall report, the tie rod fasteners used to connect the brake master cylinder to the brake booster may have been improperly fastened, resulting in unsecured or absent tire rod nuts. Due to the missing parts, the tire rods can sustain uneven pressure and bend or break when the brake pedal is applied, causing the master cylinder to detach from the brake booster.While no accidents or injuries have been reported in relation to the recall, Honda has received at least two warranty claims related to the issue.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 COMPENSATIONThe Honda and Acura recall impacts approximately 124,077 vehicles, including;2020 โ 2021 Honda Civic2020 โ 2023 Honda Ridgeline2021 โ 2023 Honda Passport2021 โ 2022 Honda Pilot2020 Acura MDXHonda expects recall notification letters to be mailed to registered owners beginning August 7, with instructions on how to schedule an appointment with an authorized Honda or Acura dealer to receive free vehicle inspection and replacement of damaged brake booster assembly components and any missing tire rod nuts.For more information on the recall, owners may contact Honda customer service by phone at 1-888-234-2138 and reference recall VEU, AEV, or ZET. They may also contact the NHTSAโs vehicle safety hotline by phone at 1-888-327-4236 (TTY 1-800-424-9153), or visit their website at www.nhtsa.gov. Tags: Auto Accident, Auto Recall, Brakes, Honda, Honda Brake RecallMore Lawsuit Stories Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis May 28, 2026 Over 3,900 Uber Sexual Assault Lawsuits Moving Forward, With Next Trial Set for Sept. 2026 May 28, 2026 Lawsuit Alleges Andexxa Administered To Reverse Xarelto Effects Caused Near-Fatal Thrombotic Event May 28, 2026 0 Comments NameThis 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 Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: today)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink 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)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: yesterday)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) GalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (Posted: 2 days ago)Growing reports of GalaFLEX breast mesh complications have raised concerns about women who required explant surgery, revision procedures or implant removal after the synthetic mesh was used during breast augmentation, breast lift, implant revision or reconstruction surgery.MORE ABOUT: BREAST MESH LAWSUITGalaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025)
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