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.
Cadillac Recall Issued Over Defective Brake Pedals That Could Fracture June 23, 2015 Irvin Jackson Add Your CommentsMore than 2,100 Cadillac vehicles have been recalled after an internal investigation by General Motors found that certain vehicles may experience brake pedal failure during normal operation, with the brake pedal assembly possibly fracturing, which may increase the risk of a crash or serious injury.ย A 2015 Cadillac ATS and CTS recall (PDF) was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) on June 3, following an investigation that led to the discovery of fracturing brake pedal assemblies installed during the manufacturing process. To date, no injuries or incident reports have been received outside of the testing facility.On March 24, 2015, officials from a GM plant reported that a 2015 model year Cadillac CTS vehicle failed the testing process due to a fracture in the bracket between the brake pedal assembly and the rod that actuates the vehicle service brakes. GM reportedly implemented a containment and inspection process for all vehicle manufactured with similar model actuators eventually leading to an investigation opened on April 22.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 automaker’s investigation determined that some of the brackets between the brake pedal assembly and rod actuator may have been fractured during the manufacturing process due to the mechanical failure of a machine.GM reported to the NHTSA that a machine used by the supplier to manufacture the affected brackets experienced a mechanical failure due to the supplier periodically using incompatible raw material in the machine. On May 27, the company determined a safety defect exists in an unknown population of the vehicles, prompting their Safety and Field Investigation Decision Authority to conduct a recall.If the brake pedal assembly fractures while the vehicle is in motion, the driver will lose the braking ability completely. This could cause fatal scenarios when approaching intersections or congested traffic-ways, posing a risk to drivers, passengers and pedestrians.The recall includes 2,163 model year 2015 Cadillac ATS and CTS vehicles manufactured by General Motors from January 27, 2015 to March 24, 2015.The NHTSA anticipates GM to begin notifying owners of the recall on August 1, 2015, which will provide customers with instructions on how to schedule an appointment at a local dealer to have the brake assembly inspected and replaced if necessary free of charge. Customers with further questions may contact Cadillacโs customer service at 1-800-458-8006 and refer to the recall number 15352. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Auto Accident, Auto Recall, Cadillac, General Motors Image Credit: Image via <a href="http://www.shutterstock.com/gallery-931246p1.html?cr=00&pl=edit-00">Ken Wolter</a> / <a href="http://www.shutterstock.com/editorial?cr=00&pl=edit-00">Shutterstock.com</a>More Lawsuit Stories Apple AirTag Stalking Lawsuits Consolidated in Northern District of California October 8, 2026 Kratom Overdose Lawsuit Alleges Krave Products Caused Fatal Mitragynine Intoxication October 8, 2026 Trifecta GT Heart Valve Lawsuit Alleges Premature Failure Led to Patientโs Death October 8, 2026 0 Comments InstagramThis 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. 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