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.
Bard Avaulta Mesh Case Census Ordered by MDL Judge January 6, 2014 Austin Kirk Add Your Comments The federal judge presiding over all vaginal mesh lawsuits has issued an order requiring a census of cases being presented by women nationwide involving injuries associated with products manufactured by C.R. Bard. There are currently more than 6,000 Bard Avaulta mesh lawsuits pending in the federal court system, which have been consolidated for pretrial proceedings as part of an MDL, or Multidistrict Litigation. The federal complaints filed throughout the country have been centralized before U.S. District Judge Joseph R. Goodwin in the Southern District of West Virginia for coordinated management during pretrial proceedings. However, additional claims are pending in various state courts and an undocumented number of cases will be presented that have not yet been filed in court. 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 In a Pretrial Order (PDF) issued December 31, Judge Goodwin indicates that “in the interest of efficient management” for the MDL, it is necessary to obtain a more accurate accounting of the number of claims being presented against C.R. Bard. Therefore, all plaintiffs’ lawyers with a lawsuit pending in the MDL are being required to register their cases by January 23, 2014. Attorneys have been directed to complete a “census spreadsheet,” providing the name of each potential plaintiff, information about the specific products used and brief details about subsequent complications experienced. This order is expected to result in a list of all potential claims Bard is facing, including claims filed in various state courts, those not yet transferred into the MDL and claims that are not yet filed in any jurisdiction. Vaginal Mesh Litigation Bard Avaulta is a type of transvaginal mesh used for repair of pelvic organ prolapse (POP) and female stress urinary incontinence (SUI). All of the claims filed in courts throughout the United States involve similar allegations that problems with the design of the product caused women to suffer severe vaginal mesh complications, including cases where the product eroded through the vagina, caused infections or other painful injuries. Judge Goodwin currently presides over six different federal MDLs that have been established for claims involving different manufacturers. In addition to cases against C.R. Bard, Judge Goodwin is managing 11,390 AMS vaginal mesh lawsuits, 11,589 Ethicon Gynecare mesh lawsuits, 7,310 Boston Scientific mesh lawsuits, 1,099 cases involving Coloplast mesh lawsuits and 133 Cook Medical mesh lawsuits. In each of the proceedings, a small group of cases have been selected for early trial dates, known as “bellwether” cases. The preparation and outcomes of these cases are designed to help the parties gauge how juries may respond to certain evidence and testimony that may be repeated throughout the litigation. The litigation involving Bard mesh products are the furthest along, with the third in a series of Avaulta bellwether trials scheduled to begin later this month, involving a lawsuit filed by Carolyn Jones. The first Bard Avaulta bellwether trial began before Judge Goodwin in July 2013, involving a complaint filed by Donna Cisson. That case ended with a jury award of $2 million in damages for the plaintiff, including punitive damages designed to punish Bard for their actions in connection with the design and sale of the transvaginal mesh. During the first day of trial in the second bellwether case, involving a complaint filed by Wanda Queen, the parties reached a settlement agreement to resolve the lawsuit for an undisclosed amount. Another trial selected for an early trial date in November was cancelled after the complaint was voluntarily dismissed by the plaintiff. The progress in the litigation and the order requiring a census of all cases may suggest that Bard is considering settling vaginal mesh lawsuits, rather than continuing to battle thousands of individuals claims over the coming years. Tags: Bard Avaulta, Bard Avaulta Mesh, Bladder Sling, C. R. Bard, 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. 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 TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Cartiva Settlement Rumors Mount Again, as More Toe Implant Lawsuits Withdrawn and Trials Approach (Posted: today) The withdrawal of two Cartiva toe implant lawsuits has sparked rumors of a potential settlement agreement to resolve product liability claims over the recalled devices. 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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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