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 Hernia Mesh Lawsuits Consolidated For Pretrial Proceedings in Federal MDL August 3, 2018 Irvin Jackson Add Your Comments The U.S. Judicial Panel on Multidistrict Litigation (JPML) has decided to consolidate all hernia mesh lawsuits filed nationwide against C.R. Bard, centralizing the cases before one judge for coordinated pretrial proceedings as part of a federal MDL, or multidistrict litigation. In an order (PDF) issued August 2, a group of 53 Bard hernia mesh lawsuits currently pending in 21 federal district courts were identified were transferred to U.S. District Judge Edmund A. Sargus in the Southern District of Ohio for coordinated discovery and management. In addition, the panel indicated that there are currently another 69 potentially related actions pending, which will soon be transferred. The lawsuits involve problems with Bard Ventralex, Bard Perfix, Bard Composix and other polypropylene hernia patch products sold in recent years. Plaintiffs raise similar questions of fact and law, alleging that design defects make the mesh prone to fail and result in the need for revision surgery within a few years. Hernia Mesh Lawsuits Did you or a loved one receive a hernia mesh? Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Hernia Mesh Lawsuits Did you or a loved one receive a hernia mesh? Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery. Learn More SEE IF YOU QUALIFY FOR COMPENSATION As lawyers continue to review potential cases for individuals who have experienced hernia mesh complications in recent years, the size and scope of the Bard litigation is expected to continue to increase in the coming months and years, and it is ultimately expected that several thousand cases may be centralized before Judge Sargus. Each of the complaints raise similar allegations that the design of the mesh products were unreasonably dangerous and defective, making them prone to fail and result in the need for risky revision surgery within a few years after the original hernia repair. On April 10, a group of plaintiffs filed a motion to centralize the Bard hernia mesh lawsuits before a single judge in the Southern District of Ohio, as part of an MDL, or multidistrict litigation. In complex product liability litigation where similar questions of fact and law are raised in complaints filed in various different U.S. District Courts, it is common for the JPML to transfer the cases to one judge for coordinated discovery into common issues, to avoid conflicting pretrial schedules from different courts and to serve the convenience of common witnesses, parties and the judicial system. C.R. Bard and Davol indicated in June that it supports centralization of the hernia mesh cases, so long as any MDL includes all lawsuits over their polypropylene mesh products, including the previously recalled Kugel hernia patch, which plaintiffs argued should be excluded from this new MDL. However, the JPML declined to address the Composix Kugel (CK) mesh cases in their decision. “Whether to include the CK Patch cases in centralized proceedings is a question not currently before the Panel, as none of the cases on the motion involve the CK Patch,” the transfer order states. “We will address this question in due course through the conditional transfer order process.” The panel ordered all of the cases centralized before U.S. District Judge Edmund A. Sargus in the Southern District of Ohio. Hernia Mesh Litigation In addition to Bard lawsuits, similar polypropylene hernia patch cases are being pursued over problems with the Atrium C-Qur patch and Ethicon Physiomesh, which have already been centralized as part of two separate multidistrict litigations (MDLs). The Atrium C-Qur, pronounced “Secure”, was approved by the FDA in March 2006, featuring a polypropylene mesh with an outer coating of gel made from 3 fatty acids. However, this design has been linked to reports of severe infections, allergic reactions and other problems. Ethicon Physiomesh was introduced in March 2010, featuring a unique, multilayered design that was intended to improve performance. However, amid a high number of failures, an Ethicon Physiomesh recall was issued in May 2016, removing the product from the market worldwide. While the action was classified as a “market withdrawal” in the United States, the manufacturer has indicated that it will not be returning the product to the market. There are currently about 1,200 Ethicon Physiomesh lawsuits and 471 Atrium C-Qur lawsuits pending in the federal court system, where they have been centralized before two separate judges for coordinated discovery. Tags: Bard, C. R. Bard, Hernia, Hernia Mesh, Kugel More Hernia Mesh Lawsuit Stories Second Bellwether Trial in Covidien Hernia Mesh Lawsuit MDL Set for July 2026 May 14, 2025 Covidien Mesh Lawsuit Set For Trial in Feb. 2026, Over Defective Hernia Implant April 10, 2025 New Bard Hernia Mesh Lawsuits Continue To Be Filed Following Global Settlement April 3, 2025 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 TermEmailThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES MDL Judge Orders Paraquat Lawsuit Settlement Update By June 11, 2025 (Posted: yesterday) A federal judge has agreed to stay all case-specific discovery deadlines in Paraquat lawsuits, while the parties work to hammer out a settlement agreement to resolve thousands of claims. 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Court Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (Posted: 2 days ago) As new Depo-Provera lawsuits continue to be filed, the judge presiding over the litigation has established key criteria for establishing proof of Depo-Provera use and medical documentation confirming a meningioma diagnosis. MORE ABOUT: DEPO-PROVERA LAWSUITDepo Shot Lawsuit Filed Over Serious Brain Tumor Injuries (05/07/2025)Lawsuit Alleges Depo-Provera Migraines, Headaches Led to Meningioma Brain Tumor Diagnosis (05/01/2025)Depo-Provera Hearing Loss Lawsuit Filed Over Brain Tumor Side Effects (04/22/2025)
BioZorb Implant Lawsuit Alleges Tissue Marker Caused Swelling, Fluid Buildup and Chronic Pain (Posted: 3 days ago) A Massachusetts woman’s injuries from a failed tissue marker that was recently recalled led to the need for physical therapy, according to a BioZorb implant lawsuit. MORE ABOUT: BIOZORB LAWSUITFour Women File BioZorb Lawsuit Over Breast Tissue Marker Failures and Injuries (05/05/2025)Lawsuit Claims BioZorb Marker Caused Chronic Pain, Multiple Surgeries After Lumpectomy (04/14/2025)Four BioZorb Breast Tissue Marker Lawsuits Selected for Bellwether Trials (04/02/2025)