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.
Initial Conference Scheduled with Judge in New Jersey Mirena IUD Litigation June 3, 2013 Austin Kirk Add Your Comments Following an order last month from the New Jersey Supreme Court to consolidate the Mirena IUD litigation pending in the state before one judge for coordinated proceedings, an initial conference has been scheduled on June 17 for the parties to meet with the Court and review the status of the lawsuits. All product liability lawsuits over Mirena IUD in New Jersey have been centralized before Superior Court Judge Brian R. Martinotti in Bergen County, as part of an MCL or Multicounty Litigation. The complaints all involve similar allegations that Bayer failed to provide adequate warnings for women or the medical community about the risk of complications from Mirena IUD, which is a small, T-shaped form of birth control that is implanted into the uterus to prevent pregnancy for up to five years. Learn More About Paragard Lawsuits Women have reported problems where Paragard IUD fractured or broken during removal, resulting in serious injury. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Paragard Lawsuits Women have reported problems where Paragard IUD fractured or broken during removal, resulting in serious injury. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Plaintiffs allege that they suffered severe injuries when the IUD perforated their uterus and migrated to other areas of the body, often resulting in damage to internal organs, infections and ultimately the need for surgery to remove Mirena. Organization of New Jersey Mirena Lawsuits According to an order (PDF) issued by Judge Martinotti, the initial conference for the New Jersey litigation has been scheduled to discuss the status of discovery in the lawsuits, the status of motions, the organizational structure of the litigation, the formation of a discovery plan, coordination with the federal MDL and to review the status of any efforts to settle Mirena lawsuits so far. Prior to the conference, counsel have been ordered to meet and confer in an attempt to seek a consensus with respect to a proposed discovery plan, suggested schedule for joinder of additional parties, amendment of pleadings, motions and trial dates. The attorneys involved have also been ordered to submit brief written statements including the status of discovery, a list of each party’s witnesses that would be expected to testify at trial, a proposed schedule for events necessary prior to trial, a concise demand or offer to resolve the lawsuits and other issues that need to be addressed by the Court. These statements are to be submitted 7 days before the conference, and will not be binding. Judge Martinoitti has also ordered that discovery continue in the cases, indicating that there will be no stay pending the conference. He also indicated that any applications for leadership positions in the state court Mirena IUD litigation should be filed seven days before the conference as well. Federal Court Mirena Litigation Status In addition to the New Jersey state court Mirena lawsuits, Bayer also faces a number of similar complaints in the federal court system. All complaints filed in U.S. District Courts throughout the country have also been consolidated for pretrial proceedings, with an MDL or Multidistrict Litigation centralized before U.S. District Judge Cathy Seibel in the Southern District of New York. Last month, lawyers were appointed to various leadership roles in the federal proceedings, which was established in April 2013. It is expected that there will be coordination between the state and federal court actions. The issues presented in the case will center on whether Bayer provided adequate warnings about the risk of “spontaneous” migrations of the Mirena IUD, where the device perforates the uterus and causes internal damage after it is inserted. While the Mirena warning label does indicate that there is a risk of perforation at the time of insertion, plaintiffs allege that the manufacturer failed to warn about the risk of severe internal damage, infections and other problems that may surface months or even years after the IUD has been in place. There are currently only about 100 lawsuits filed throughout the country, but the size of the Mirena litigation is expected to continue to increase over the coming year as lawyers investigate and file new cases, as thousands of women have reported problems involving Mirena. More Mirena Lawsuit Stories Link Between Mirena IUD and Breast Cancer Side Effects Strengthened in New Study October 18, 2024 Mirena IUD Class Action Lawsuit Over Breast Cancer Risk Cleared to Move Forward October 12, 2023 Mirena IUD Breast Cancer Risk Results in Class Action Lawsuit Against Bayer March 17, 2022 0 Comments LinkedInThis 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: 2 days ago) 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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