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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Ingenio Pacemaker, CRT-P Recall Issued After Dozens of Incidents and Patient Injuries August 9, 2021 Russell Maas Add Your Comments Following reports of severe and potentially life-threatening injuries, a recall has been issued for certain Boston Scientific pacemakers, which may suddenly stop providing critical heart pacing therapy. The FDA announced a Boston Scientific INGENIO pacemaker recall on August 6, indicating there have been at least 65 reports of the pacemakers suddenly switching to “safety mode”, causing a loss of pacing or ability to regulate the patient’s heart rate. Pacemakers are implantable devices positioned under the skin and are designed to assist the heart’s pumping action to treat fast, irregular, or slow heart rhythms, by applying small electric pulses to either one or both sides of the heart to keep the left and right chambers beating in proper sync. The devices are also used to treat patients susceptible to heart failure by improving the body’s ability to pump blood and distribute oxygen. Do You Know about… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The recall includes Boston Scientific’s INGENIO family of pacemakers and CRT-Ps marked with model numbers J174, J177, K174, K184, and K187 and product code LWP. The devices were manufactured by Boston Scientific of Marlborough, Massachusetts from November 1, 2011 through August 1, 2020. About 48,000 devices are affected. According to an Important Medical Device Advisory issued by Boston Scientific on June 3, the manufacturer knows of at least 65 incidents, including three serious injuries, in which the pacemakers have incorrectly and suddenly transitioned to safety mode, which is intended to provide backup functionality if the device is faulty. No deaths have been linked to the malfunction. The FDA warns that when the device unintentionally switches to safety mode there could be a reduced pacing ability and inability to regulate a patient’s heart rate, which could lead to serious or life threatening injuries. If the device goes into safety mode, the device cannot be reprogrammed, requiring early device replacement procedures, officials warn. Boston Scientific and the FDA do not recommend proactively replacing the pacemakers at this time, and replacement procedures should only occur if the device experiences the defect and switches to safety mode on its own. The agency and the manufacturer are asking healthcare professionals to assess specific patient risk factors including underlying health issues, pacemaker dependence, or problems with pacing to prevent unintended outcomes. Patients with the recalled pacemakers should be closely monitored and have a system follow-up remotely or in person at least every 12 months, according to Boston Scientific’s recommendations. The FDA has categorized the recall as a Class I recall, indicating it is the most serious of its kind, and that the use of the device has a high probability of causing severe patient injury or death. The FDA requests any health care professionals or patients who experience a problem with the recalled pacemakers file a report with the FDA’s MedWatch adverse event reporting program. Tags: Boston Scientific, Heart Rhythm, Pacemaker, Pacemaker Recall More Lawsuit Stories Suboxone Injury Lawyers Reappointed to Leadership Roles in Federal MDL July 14, 2025 $27 Million PFAS Water Contamination Settlement Reached By DuPont in New York Lawsuit July 14, 2025 Rent Fixing Lawsuit Filed Against RealPage and Landlords Over Property Management Software July 14, 2025 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Suboxone Injury Lawyers Reappointed to Leadership Roles in Federal MDL (Posted: today) A federal judge has confirmed the reappointment of more than two dozen Suboxone injury lawyers to serve in leadership positions representing plaintiffs for another year. 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