Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
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.
St. Jude Defibrillator Battery Settlement Resolves Class Action Lawsuit in Canada August 8, 2019 Austin Kirk Add Your Comments St. Jude Medical has agreed to pay $5 million to settle a class action lawsuit in Canada, resolving claims over battery failures in a number of its implantable cardiac defibrillators. The problems impacted certain St. Jude Fortify, Fortify Assura, Quadra Assura, Unify, Unify Assura and Unify Quadra devices, and the manufacturer has faced a number of claims that allege the batteries may deplete prematurely due to a manufacturing defect that results in the formation of lithium clusters. The St. Jude defibrillator battery settlement was approved by the Ontario Superior Court of Justice on August 7, allowing any person implanted with the affected devices in Canada to make a claim for compensation. Close family members can make wrongful death claims if they can establish the death was due to battery failure in the devices. 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 In the United States, a number of injury and wrongful death lawsuits following a St. Jude Implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) recall announced by the FDA in October 2016. That recall came after at least two deaths and dozens of adverse event reports have been linked to the St. Jude battery problem. Months after the recall, the FDA sent a warning letter to St. Jude and it’s new parent company, Abbott Laboratories, warning that some devices were still shipped out after the recall, with at least seven patients implanted with defibrillators that were then known to be defective. St. Jude has continued to have ICD battery problems in its devices. In April 2018, the company had to issue a firmware update to address additional battery issues, which the FDA declared a recall. Many of the same devices were affected. In lawsuits over St. Jude defibrillator battery problems filed throughout the U.S., plaintiffs allege that the manufacturer knew about the potential risks associated with their product as early as 2011, but continued to distribute implants they knew could fail prematurely. Nearly 9,000 Canadians received the implants and may be eligible for compensation for the settlement there. They can visit www.stjudeicdclaim.ca for more information. Tags: Abbott Laboratories, Battery, Canada, Class Action Lawsuit, Defibrillator, ICD, St. Jude More Lawsuit Stories Wayfair Fire Pit Lawsuit Links Flame Jetting Explosion to Defective Design September 5, 2025 Woman Files Trulicity and Ozempic Lawsuit Over Ileus, Intestinal Obstruction September 5, 2025 Cigarette Smoke May Accelerate Silicosis Risks: Study September 5, 2025 5 Comments Jeffrey January 2, 2022 I have or I had a implancable cardioverter defibrillator But it went bad burn a hole in my chest It called an infection in my body I had to stay in the hospital a week So yes please give me a call my phone number is 8175501291 So yes please give me a call my heart rate is going plump out of sight bomb outside it’s just a matter of time before I have a heart attack because I do not have an AICD, ANYMORE, Tanisha April 30, 2021 I would like to have a lawyer to help me with my defective battery Ursula December 31, 2020 In November 2013 an implantable defibrillator/pacemaker was my birthday present for heart failure. By April 2014, I was back in the hospital because the devise caused pain and frozen shoulder syndrome. Not only did I need therapy to replace the site of the floating defibrillator, but I was also put through a lot by the hospital on this situation. As if I had caused this to happen to myself, geez. I was told by the Pain Management Doctor that the devise was floating on the outside near nerves that caused my frozen shoulder and black outs. Of course she didn’t note it… I just saw her look at her shoes while she said that. Yes, I said “Blackouts”. Nothing was ever done with an exception of a psychological test on me. I guess the person(s) who wanted that one was totally disappointed. Anyway, St. Jude is still implanted in me to this day. Because I’m at a county hospital, they’re speaking on reinserting the same devise with better technology within a year or two. I still have pain from this devise, please. Somewhat relief comes Lidocaine cream and therapy. I’m done with therapy! Please help me. Susan January 13, 2020 My husband had the st jude defibrillator put in on Jan 14,2015 his no# was in this recall looking for someone to listen and get compensation for this . No one let us know that this was in a recall .he passed away on October 23 2016! Sincerely Susan Gruber dennis October 4, 2019 My name is Dennis Doss. I am 63 years old and on disability for heart problems. I had a St. Jude pacemaker replaced in December of 2017 that I later found out was on the recalled device list. It was placed in me in May of 2015 and replaced 2 ½ years later for battery problem. During that 2 ½ year time, I was hospitalized 6 times for pulmonary edema and subsequent cardiac ablations for ventricular tachycardia that my pacemaker could not pace me out of. During some of those visits, I was manually shocked to regain a normal heart rhythm. The 2015 St. Jude ICD was a three lead model. Apparently, there was a problem with one of the leads. (It was drawing too much power) I understand there are some known problems with leads as well. In 2017, the new pacemaker my doctor installed only required 2 leads, so the 3rd defective lead was left inside me and not used. My doctor said that it was more dangerous to me to remove it than to just leave it in and unused. I don’t know if any of this qualifies me for a case against St. Jude, but I had a very rough 2 ½ years while having that pacemaker in me. My new ICD is made by a German company, Biotronik. Since its installation, I have had no recurring problems with my heart at all. Thank you for your attention to this matter. 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. 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