Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study
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.
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.
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.
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.
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.
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.
Ocaliva Lawsuit Ocaliva lawsuits are being investigated for users who experienced liver failure, cirrhosis progression, transplant, or death after taking the drug, alleging that Intercept Pharmaceuticals failed to warn about the risk of dosing toxicity and accelerated liver damage.
Roblox Lawsuit Families are filing Roblox lawsuits after children were targeted by predators for grooming, sextortion, sexual abuse, or exploitation on the platform. Learn who qualifies, what cases allege, and how to file a confidential claim.
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.
JPML To Hear Neomedic Vaginal Mesh Consolidation Arguments Jan. 30 January 3, 2014 Austin Kirk Add Your Comments The U.S. Judicial Panel on Multidistrict Litigation (JPML) has scheduled oral arguments for January 30 to consider a motion to consolidate and centralize all Neomedic vaginal mesh lawsuits filed in U.S. District Courts nationwide. The lawsuits are by women who suffered complications from implants meant to treat pelvic organ prolapse and stress urinary incontinence. There are currently more than 35,000 product liability lawsuits pending throughout the federal court system involving problems with transvaginal mesh or bladder sling products made by various different manufacturers. The U.S. JPML has previously established six different MDLs, or multidistrict litigations, involving lawsuits filed against C.R. Bard, American Medical Systems (AMS), Ethicon, Boston Scientific, Coloplast and Cook Medical. Each of the consolidated pretrial proceedings are centralized before U.S. District Judge Joseph Goodwin in the Southern District of West Virginia to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings from different judges and to serve the convenience of the parties, witnesses and the courts. 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 According to a Notice of Hearing Session (PDF) issued last week, the panel has scheduled oral arguments on a request filed to establish a seventh MDL before Judge Goodwin for all Neomedic needleless sling lawsuits. There are currently at least 21 complaints pending against Neomedic in eight different U.S. District Courts. The cases raise nearly identical allegations to claims made against the other manufacturers, indicating that the design of the pelvic repair products were not adequately researched and that inadequate warnings were provided about the risk of complications where the mesh may erode through the vagina, cause infections or other painful injuries. Plaintiffs filed the request to establish a Neomedic mesh MDL last month, asking that all product liability lawsuits involving the Neomedic Needleles sling, Contasure Needleless sling and Remeex System be included. Neomedic has opposed the tranfer request, maintaining that centralizing the cases as part of an MDL would be detrimental to the progress of cases already filed. Vaginal Mesh Litigation Status According to the latest case list (PDF) released by the U.S. Judicial Panel on Multidistrict Litigation on December 16, in the federal court system there are currently 11,589 Ethicon Gynecare mesh lawsuits, 11,390 American Medical System (AMS) mesh lawsuits, 7,310 Boston Scientific mesh lawsuits, 5,505 Bard Avaulta mesh lawsuits, 1,099 Coloplast bladder sling lawsuits and about 133 Cook Medical biologic mesh lawsuits. In many of those MDLs, Judge Goodwin has scheduled a series of early trial dates, known as “bellwether” cases, which are designed to help the parties gauge how juries are likely to respond to certain evidence and testimony that will be repeated throughout a number of similar cases. At least four pelvic mesh cases have already reached trial, with two cases going before state court juries and two cases proceeding to trial in federal court. In July 2012, a California state court jury awarded $5.5 million in damages against C.R. Bard and a New Jersey state court jury awarded $11.1 million in damages against Ethicon in March 2013. In July 2013, a federal jury awarded $2 million in damages against Bard, including punitive damages designed to punish the manufacturer for their actions surrounding the design and sale of Avaulta pelvic mesh products. A second Bard case settled during the first day of trial for an undisclosed sum. Next year, additional trials are expected to begin against Bard, AMS, Boston Scientific and Ethicon. About one case per month will begin before Judge Goodwin between January 2014 and September 2014. Following the bellwether cases, if vaginal mesh settlement agreements are not reached by the manufacturers to resolve a large number of cases, hundreds of individual lawsuits could be set for trial dates throughout the country. Tags: Bladder Sling, Neomedic, Pelvic Mesh, 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 PhoneThis field is for validation purposes and should be left unchanged.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 Term Δ MORE TOP STORIES GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director (Posted: today) Former Becton Dickinson safety officer Dr. Hooman Noorchashm warns that the company’s GalaFLEX mesh is being used off-label in breast reconstruction without FDA approval, as lawsuits investigate whether the manufacturer failed to warn about its potential risks. 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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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