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.
Stryker Settlement for Recalled Hip Implants to Move Forward with Payments May 10, 2017 Austin Kirk Add Your Comments Claimants participating in a Stryker settlement for recalled Rejuvenate and ABG II hip implants should begin receiving compensation by the end of this year, under an expanded deal announced late last year for individuals who required revision surgery prior to December 19, 2016. A recall for Stryker Rejuvenate and ABG II modular hips impacted tens of thousands of individuals nationwide in July 2012, after the manufacturer acknowledged that a higher than expected number of implants were catastrophically failing, often as a result of fretting or corrosion at the point where the two metal pieces fit inside each other. The longer the recalled hip implants remain in individuals’ bodies, the number of failures has continued to increase, causing more and more individuals to undergo risky revision surgery to have the dangerous device removed and replaced. Learn More About Stryker Rejuvenate Hip Lawsuits Lawsuits for problems with recalled Stryker Rejuvenate and ABG II hip implants. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Stryker Rejuvenate Hip Lawsuits Lawsuits for problems with recalled Stryker Rejuvenate and ABG II hip implants. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Following several years of litigating Stryker Rejuvenate and ABG II lawsuits, the manufacturer originally announced a settlement in late 2014, which resolved all claims involving a revision on or before November 2, 2014. Under that Stryker settlement agreement, an average base payment of $300,000 was provided for each plaintiff, with several factors that may reduce the base award or increase it. At the end of last year, the manufacturer agreed to expand the Stryker Rejuvenate and ABG II settlement, making individuals who required revision surgery through December 19, 2016 eligible for compensation. According to a statement released by Stryker Corporation this week, 95% of additional eligible claimants have enrolled in the Settlement Program. As a result, the manufacturer will move forward with the second phase of the deal, indicating that the majority of all compensation payments will be made by the end of 2017. As additional Stryker Rejuvenate and ABG II implants fail in the coming months and years, it is widely expected that the manufacturer will need to expand the settlement again in the future. The resolution of these cases stemming from the 2012 hip recall come as a new round of Stryker hip lawsuits begin to mount over problems with recalled LFit V40 femoral heads, which were removed from the market last year amid reports of loosening, instability, disassociation and other problems. In August 2016, Stryker sent a notice to orthopedic surgeons about reports of problems with certain large diameter femoral heads, which are commonly used with Stryker Accolade hip stems, as well as other components. As a growing number of these new hip replacement lawsuits have been filed throughout the federal court system involving implants with the LFit V40 femoral head, the U.S. Judicial Panel on Multidistrict Litigation (JPML) established consolidated pretrial proceedings last month, centralizing the cases before U.S. District Judge Indira Talwani in the District of Massachusetts for coordinated discovery and bellwether trials, as part of a federal MDL, or Multidistrict Litigation. If the manufacturer fails to reach another Stryker hip settlement to resolve the LFit cases, each of the cases may later be remanded back to U.S. District Courts nationwide for separate trial dates. Tags: Hip Replacement, Stryker, Stryker ABG II, Stryker LFit, Stryker Rejuvenate Image Credit: | More Stryker Rejuvenate Hip Lawsuit Stories Stryker Hip Settlement Covers Additional Recalled Rejuvenate, ABGII Implants December 21, 2016 Stryker Hip Implant Failures May Be Caused by LFIT V40 Femoral Head, Manufacturer Warns October 7, 2016 Stryker Rejuvenate Hip Revision Surgery Often Leads To More Complications: Study December 4, 2015 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 Lawsuit Alleges Depo-Provera DMPA Injection Increases Brain Tumor Risks (Posted: 2 days ago) A Depo-Provera lawsuit blames the active ingredient, DMPA, for an increased risk of the development of brain tumors. 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Stryker Hip Implant Failures May Be Caused by LFIT V40 Femoral Head, Manufacturer Warns October 7, 2016
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