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.
Uncertainty Surrounds St. Jude Riata Lead Replacement Expenses, Safety August 27, 2012 Austin Kirk Add Your Comments Patients implanted with recalled St. Jude Riata defibrillator leads could face significant costs and uncertainty in having the wires removed and replaced, especially if they elect to have the lead replaced under the warranty provided by the manufacturer. Â Since a St. Jude Riata lead recall was issued last year for the small wires used to connect implantable defibrillators to the heart, doctors and patients have faced a tough decision about whether they should have the leads removed or leave them in place, as the replacement surgery can be very risky and expensive. The St. Jude Riata was recalled after it was discovered that the lead wires may poke through the insulation, potentially resulting in unnecessary electrical shocks or causing the defibrillator to fail to work when it is needed to return the heart to a normal rhythm. Learn More About St. Jude Riata Lead Lawsuit A St. Jude Riata defibrillator lead recall was issued due to a risk of insulation failure. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About St. Jude Riata Lead Lawsuit A St. Jude Riata defibrillator lead recall was issued due to a risk of insulation failure. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Earlier this month, the FDA indicated that individuals who still have one of these defective leads implanted should obtain x-rays or other imaging exams to check for problems with their Riata leads. Despite the risks associated with removing the lead, a growing number of patients are opting to have their St. Jude Riata lead replaced with a different lead. According to a recent report in the Wall Street Journal, St. Jude Medical is agreeing to honor the 5-year warranty on the Riata leads, paying $600 for each lead removed, plus providing a free St. Jude Durata defibrillator lead as a replacement. However, it appears that individuals must elect to receive this newer St. Jude lead to qualify for the warranty, which is causing concerns for many. Concerns About Safety of Newer St. Jude Durata and Riata ST Optim Leads The newer St. Jude defibrillator leads feature a redesigned insulating material, with a mix of silicone and polyurethane, which the manufacturer calls “Optim”. However, concerns have surfaced that the St. Jude Durata lead and Riata ST Optim, which feature this new insulating material, may be at risk of suffering similar problems where the lead conductors may become externalized. According to a study published last week in the medical journal Europace, researchers indicated that similar insulation problems may impact these newer St. Jude defibrillator leads as well. Researchers identified at least 52 reports of problems with St. Jude Durata and Riata ST Optim leads in the FDA’s Manufacturers and User Device Experience (MAUDE) database, including at least one death attributed to the insulation problems with the new St. Jude defibrillator leads. In an FDA safety communication issued August 16, the federal regulatory agency indicated that St. Jude had been ordered to conduct a battery of new clinical studies to help the agency truly assess the insulation problems. The manufacturer has been ordered to conduct a three-year postmarket surveillance study to look at the risk of premature insulation failure not only on the recalled leads, but also on the newer St. Jude Durata and Riata ST Optim leads. As a result of the problems, many doctors are recommending patients replace St. Jude Riata leads with defibrillator leads made by different companies, such as Boston Scientific. However, according to the Wall Street Journal, this would void the terms of the warranty provided with the recalled Riata leads. Compensation and Settlements for Replacement of St. Jude Riata Defibrillator Leads It has been reported the St. Jude is considering individual settlements and reimbursements for Riata lead replacements above the warranty cost on a case-by-case basis. However, few details have been provided about what they are voluntarily agreeing to pay, and there is no indication that the company is willing to pay any non-economic damages, such as pain and suffering associated with a St. Jude Riata replacement. A number of individuals who received the recalled leads are now consulting with product liability lawyers investigating St. Jude Riata claims to make sure they obtain all of the compensation they may be entitled to. In recent months, a number of St. Jude Riata lead lawsuits have been filed by individuals who experienced problems with insulation on their lead, seeking compensation through the court system. The complaints allege that St. Jude failed to manufacture the leads consistent with the FDA approved processes, which may cause the insulation to wear thinner at certain parts due to friction and abrasion. Tags: Defibrillator, Durata, ICD, Riata, St. Jude More St. Jude Riata Lead Lawsuit Stories Leadless Pacemakers May Have Lower Complications Rates: Study October 20, 2021 St. Jude Defibrillator Lawsuit Alleges Device Failure Resulted in Fatal Auto Accident October 5, 2017 Implanted Defibrillators Linked To High Risk Of Complications: Study May 9, 2016 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 12 Hair Dye Lawsuits Over Bladder Cancer Risks Assigned to One Judge in California State Court (Posted: today) A dozen hair dye lawsuits over bladder cancer risks have been consolidated under one California state judge for coordinated pretrial proceedings. MORE ABOUT: HAIR DYE LAWSUITJudge To Meet With Hair Dye Lawyers in Bladder Cancer Lawsuit for Initial Status Conference (06/16/2025)Lawsuit Claims Paul Mitchell, Redken, Other Hair Dyes Led to Bladder Cancer Diagnosis for Hairdresser (05/09/2025)Salon Stylist Files Lawsuit Over Bladder Cancer From Hair Dye Products (05/02/2025) BioZorb Implant Removal Surgery: What Women Need To Know When the Device Fails To Dissolve (Posted: yesterday) Following a Class I recall, more than 100 BioZorb lawsuits have been filed by breast cancer survivors who suffered painful complications after the surgical tissue marker failed to dissolve as intended. 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St. Jude Defibrillator Lawsuit Alleges Device Failure Resulted in Fatal Auto Accident October 5, 2017
12 Hair Dye Lawsuits Over Bladder Cancer Risks Assigned to One Judge in California State Court (Posted: today) A dozen hair dye lawsuits over bladder cancer risks have been consolidated under one California state judge for coordinated pretrial proceedings. MORE ABOUT: HAIR DYE LAWSUITJudge To Meet With Hair Dye Lawyers in Bladder Cancer Lawsuit for Initial Status Conference (06/16/2025)Lawsuit Claims Paul Mitchell, Redken, Other Hair Dyes Led to Bladder Cancer Diagnosis for Hairdresser (05/09/2025)Salon Stylist Files Lawsuit Over Bladder Cancer From Hair Dye Products (05/02/2025)
BioZorb Implant Removal Surgery: What Women Need To Know When the Device Fails To Dissolve (Posted: yesterday) Following a Class I recall, more than 100 BioZorb lawsuits have been filed by breast cancer survivors who suffered painful complications after the surgical tissue marker failed to dissolve as intended. MORE ABOUT: BIOZORB LAWSUITLawsuit Claims Biozorb Implant Penetrated Skin, Causing Massive Infection (06/04/2025)Breast Cancer Survivors File BioZorb Tissue Marker Lawsuit After Implant Fails (05/20/2025)BioZorb Implant Lawsuit Alleges Tissue Marker Caused Swelling, Fluid Buildup and Chronic Pain (05/14/2025)
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