Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study
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.
Coloplast Mesh Lawyers Appointed to Leadership Roles in MDL September 27, 2012 Austin Kirk Add Your Comments Following the first status conference held earlier this month in the recently established multidistrict litigation (MDL) for all Coloplast vaginal mesh lawsuits filed throughout the federal court system, lawyers have been assigned to serve in various leadership roles, where they will have responsibility for performing certain actions that benefit all plaintiffs. On August 6, the U.S. Judicial Panel on Multidistrict Litigation established an MDL for the Coloplast mesh litigation, consolidating cases throughout the United States that have been brought by women who allege they experienced severe injuries and vaginal mesh complications from products manufactured and sold by Coloplast Corp. The lawsuits have been centralized before U.S. District Judge Josephe R. Goodwin in the Southern District of West Virginia, where four other vaginal mesh MDLs are already pending for Bard Avaulta mesh lawsuits, American Medical Systems (AMS) mesh lawsuits, Boston Scientific mesh lawsuits and Ethicon mesh lawsuits. Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION All of the complaints involve similar allegations that vaginal mesh and bladder sling products sold for surgical repair of pelvic organ prolapse (POP) and female stress urinary incontinence (SUI) were defective and dangerous. Plaintiffs allege that the products were not adequately researched or tested, and that proper warnings were not provided about the risk of painful and debilitating problems, such as erosion of the mesh through the vagina, infection and pelvic pain. Organization and Structure of Vaginal Mesh MDLs Consolidation and centralization of complex product liability lawsuits for pretrial proceedings is common in the federal court system, as it reduces duplicative discovery, eliminates contradictory pretrial rulings from different judges and serves the convenience of the parties, witnesses and the courts. However, it is unique to have multiple different MDLs established before one judge, which involve nearly identical products manufactured by different companies. In April 2012, after the AMS, Boston Scientific and Ethicon MDLs were assigned to Judge Goodwin, three other attorneys were appointed to serve as Coordinating Co-Lead Counel, working across MDL lines to coordinate which other attorneys are best suited to handle tasks that will be common to lawsuits filed against all defendants. In addition, individuals groups of Co-Lead Counsel were appointed in each of the MDLs, with one large Plaintiffs’ Steering Committee (PSC) established to divide up duties during pretrial proceedings and discovery involving evidence common to all cases. At that time, 60 lawyers were appointed to serve on the joint vaginal mesh plaintiffs steering committee. Coloplast Mesh Lawsuits are Fifth MDL Before Judge Goodwin After the fifth MDL was established for the Coloplast mesh, Judge Goodwin met with attorneys involved in those cases for the first time on September 13, to discuss the organization and structure of the litigation. In a pretrial order (PDF)Â issued on September 21, Judge Goodwin appointed three Coloplast mesh lawyers to serve as co-lead counsel for plaintiffs, including Riley Burnett, Jr., Mark Mueller and Robert Salim. These attorneys will act as the spokesperson for all plaintiffs at pretrial proceedings and in response to any inquiries by the court. They will also submit and argue motions, examine witnesses, introduce evidence at pre-trial hearings and be responsible for negotiating any stipulations or settlements that apply to all cases, among other duties. The remaining leadership structure across all of the vaginal mesh MDLs was not changed, with no additional lawyers appointed to the Plaintiff’s Executive Committee or Plaintiffs’ Steering Committee. With regard to the discovery plan in the lawsuits, the parties advised Judge Goodwin at the conference that they are working on an early assessment plan and that Coloplast Corp. has entered into tolling agreements with a number of plaintiffs. While Judge Goodwin indicated that he was willing to issue a temporary stay on discovery in the Coloplast mesh lawsuits, to allow the parties to develop a discovery plan, he indicated that he intends to move the MDL forward to make sure it does not fall too far behind the others. Therefore, the parties were allowed to engage in informal agreed upon discover, and no orders will be entered before the next status conference requiring discovery of either party. The next status conference is currently scheduled for November 2, with additional conferences set for January 10, 2013 and February 7, 2013. Tags: AMS Vaginal Mesh, Bard Avaulta, Bladder Sling, Boston Scientific Pinnacle Mesh, Coloplast, Ethicon, Gynecare, Gynecare Prolift, Mentor, Transvaginal Mesh, Vaginal Mesh More Vaginal Mesh Lawsuit Stories Study Finds Some Transvaginal Mesh Degrades Within 2 Months After It Is Implanted October 29, 2024 Supreme Court Rejects J&J Bid to Overturn $302M Vaginal Mesh Lawsuit Award February 23, 2023 Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study January 16, 2023 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. 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Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study January 16, 2023
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