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.
MDL Sought for Stryker Recall Lawsuits Over LFit v40 Hip Implants January 23, 2017 Austin Kirk Add Your Comments With a growing number of Strkyer LFit V40 hip lawsuits being filed throughout the federal court system over the recalled femoral head component, a request has been filed to consolidate the litigation for centralized pretrial proceedings. A motion (PDF) was filed with the U.S. Judicial Panel on Multidistrict Litigation (JPML) by plaintiffs on January 13, seeking to transfer cases pending in U.S. District Courts nationwide to one judge for coordinated discovery, pretrial motions and a series of bellwether trials. There are currently only about six product liability lawsuits filed over problems linked to the Stryker LFit v40 femoral head, which was removed from the market last year due to an increased risk of premature failure, corrosion and cobalt metal blood poisoning. However, as hip replacement lawyers continue to review and file claims for individuals who had to undergo revision surgery after receiving the implant, it is expected that hundreds of additional lawsuits may be filed in the coming months and years. Learn More About Hip Replacement Lawsuits Lawsuits are being reviewed for several different dangerous and defective hip replacement systems. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Hip Replacement Lawsuits Lawsuits are being reviewed for several different dangerous and defective hip replacement systems. Learn More SEE IF YOU QUALIFY FOR COMPENSATION “Plaintiffs contend that Stryker knew for years that the LFIT V40 femoral heads were defective and dangerous but instead chose to downplay the risk of using such device and failed to properly warn the hundreds of physicians implanting these devices into thousands of patients across the country,” the motion filed by plaintiff Robert O’Hare states. “Plaintiffs further claim that the LFit V40 femoral head was defectively designed, manufactured and marketed by the defendants resulting in serious and significant injury to consumers.” The motion suggests that all of the cases and any future lawsuits involving similar claims be transferred to the U.S. District Court for the District of Massachusetts to reduce duplicative discovery into common issues in the cases, avoid conflicting pretrial rulings and to serve the convenience of the parties, witnesses and the judicial system. Stryker LFit V40 Hip Recall A Stryker LFit V40 recall was first announced as part of a hazard alert issued by Australia’s Therapeutic Goods Administration, indicating that certain large-diameter femoral heads manufactured before 2011 may experience taper lock failures, which can result in loss of mobility, pain, inflammation, adverse local tissue reactions, dislocation and the need for revision surgery, among other complications. The action was taken after an investigative report published in the Journal of Bone and Joint Surgery in August 2016, which outlined five cases of catastrophic failure with Stryker Accolade and LFit V40 combinations, which noted that there was extensive corrosion in the V40 head and Accolade stem that caused the stem to fracture at the stem/head juncture. In 2014, the first Stryker hip lawsuits were filed by individuals who experienced problems after receiving an Accolade hip implant together with the LFit V40 femoral head, alleging that the components were defectively designed and manufactured. If the cases are consolidated as part of a federal MDL, all pending and future cases will be transferred to one judge. However, if Stryker hip recall settlements are not reached following the coordinated discovery and any bellwether trials, each individual complaint may be remanded back to the court where it was originally filed for an individual trial date in the future. The U.S. JPML is expected to consider oral arguments on the motion during an upcoming hearing set for March 30, in Phoenix, Arizona. Tags: Hip Replacement System, Stryker, Stryker Accolade, Stryker LFit More Hip Replacements Lawsuit Stories Biomet Hip Lawsuit Filed Over Defective M2A Metal-on-Metal Implant December 26, 2024 Zimmer Biomet Lawsuit Filed Over RibFix Blu Implant Fracture September 25, 2024 Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024 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 TermNameThis 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: 3 days ago) 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. MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSParaquat Settlement Reached for Parkinson’s Disease Lawsuits Filed in MDL (04/16/2025)Appeals Court Urged To Reinstate Paraquat Lawsuits Previously Set for Bellwether Trials (02/14/2025)Paraquat Lawsuits Over Parkinson’s Disease Risk Set for Trial in October 2025, April 2026 (01/29/2025) Court Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (Posted: 4 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. 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Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
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Court Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (Posted: 4 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: 5 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)