Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
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.
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.
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
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.
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.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
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.
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.
Exactech Knee and Hip Implant Lawsuit Bellwether Plan Proposed for MDL and Florida State Court LitigationExactech faces more than 1,000 hip and knee implant lawsuits in federal and state courts nationwide, according to court documents. August 14, 2023 Irvin Jackson Add Your CommentsA proposed bellwether plan has been submitted that calls for a group of Exactech knee implant lawsuits and hip implant lawsuits to be prepared for early trial dates in the federal multidistrict litigation (MDL) and Florida state court, which may help gauge how juries are likely to respond to certain evidence and testimony that will be presented throughout hundreds of claims being pursued by individuals nationwide.Exactech currently faces at least 1,131 product liability lawsuits, each raising similar allegations that โout-of-specificationโ vacuum sealed bags were used with a plastic tibial insert component in recent years, allowing oxygen to reach the knee, hip and ankle implants long before they were placed in the body. This has been shown to increase the risk of degradation and premature failure, often resulting in the need for additional surgery to remove the component only a few years later.The litigation emerged after anย Exactech recallย was issued in February 2022, impacting more than than 140,000 Optetrak, Optetrak Logic and Truliant knee replacement systems implanted in patients since 2004, as well as 1,500 components used in Exactech Vantage ankle replacements. Similar packaging problems have also impacted Exactech Novation and Acumatch hip implants since 2008, which were recalled in June 2021, and theย Exactech hip recall was expandedย in August 2022, to add another 40,000 joint replacements that may fail prematurely.Learn More AboutKnee Replacement LawsuitsIf you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutKnee Replacement LawsuitsIf you or a loved one experienced complications or required revision surgery due to a defective knee replacement implant, you may be entitled to financial compensation.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONGiven common questions of fact and law raised in the complaints filed throughout the federal court system, consolidated pretrial proceedings have been established before U.S. District Judge Nicholas G. Garaufis in the Eastern District of New York, for coordinated discovery and pretrial proceedings.According to a joint status report (PDF) submitted by the parties on August 11, there are currently at least 822 claims pending in the federal Exactech MDL, of which 665 involve problems with knee implants, 146 involve Exactech hip lawsuits, and only 10 involve ankle replacement products.However, there are another 272 Exactech lawsuits pending in Florida state courts, where the manufacturer’s U.S. headquarters are located. Of the Florida state court litigation, there are 191 Exactech knee lawsuits, 77 hip failure lawsuits, and four ankle failure lawsuits. There are also another 14 cases filed in Illinois and 23 claims scattered across various other state courts nationwide, according to the status update.Exactech Knee and Hip Lawsuit Bellwether PlanThe parties submitted the updated information about the numbers of claims pending nationwide ahead of a status conference later this month before Judge Garaufis, which is scheduled for August 22.As part of the management of the litigation, Judge Garaufis has indicated he will schedule a small number of representative claims for early test trials, to help gauge how juries are likely to respond to certain evidence and testimony that will be repeated throughout the claims. Earlier this year, he called for parties to propose an Exactech bellwether plan for the selection and preparation of those cases for the first federal trials.The parties submitted their proposal (PDF) on July 28, calling for close coordination with the Florida state court judge presiding over that litigation. As presented, the parties called for the first two Exactech hip implant lawsuits to be held in Florida state court, with the first two Exactech knee implant lawsuits to be held in federal court.โIn an effort to facilitate coordination of discovery and even more ambitiously, of a coordinated bellwether plan, the parties were able to negotiate across the coordinated jurisdictions and reach a novel and innovative joint bellwether plan between the jurisdictions,โ the joint proposal states. โLead counsel for the parties in the MDL and in Florida agree that the plan is sensible and efficient by sparing all parties the extreme costs of full-fledged work up and preparation for trial of a large number of cases, concentrating the bellwether pools by product and addressing the complex venue and choice of law issues that come with national litigation such as this.โThe joint proposal notes that the Florida state court cases have a much higher proportion of Exactech hip lawsuits, when compared to the federal MDL. In addition, some of those hip lawsuits filed at the Florida state level have already been through much of the process to prepare them to go before a jury. The federal MDL, by comparison, has only a small fraction of cases that are not Exactech knee lawsuits.For the federal bellwether pool, the parties call for two groups of cases to be selected, one involving 12 cases chosen from around the country, and another consisting of 12 cases that were originally filed in the Eastern District of New York, where Judge Garaufis can preside over trials without venue waivers.Those two pools would later be reduced down to four cases each, including a total of eight cases that will be eligible for the first trials. Each side would then recommend two Exactech lawsuits from the National Pool and two from the New York Pool for the first bellwether trials, and Judge Garaufis would then select two cases from each pool to go before juries in the federal court system.For the Florida state court litigation, the proposal calls for a separate group of 12 cases to be selected, with each side choosing two cases, and the remaining eight cases being selected randomly by the Court. After discovery, each side would have the ability to strike four cases from the pool, and the state court judge would select two cases for trial from the remaining four Florida Pool selections.Judge Donna Keim of the Eighth Judicial Circuit is currently overseeing the Exactech lawsuits in Florida state court, and has previously indicated that the first case will go to trial in the state in October 2024. However, there has not yet been a trial date set in the federal MDL.Although the outcomes of any bellwether trials in the federal MDL or Florida state court will have no binding impact on other lawsuits in the litigation, they will be closely watched and may have a large impact on any Exactech recall settlements the manufacturer offers to avoid the need for hundreds of individual trials to be scheduled in the coming years. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Exactech, Florida, Knee Implant, Knee Implant Recall, Knee Replacement System, OptetrakMore Knee Replacement Lawsuit Stories Exactech Implant Settlement Results in $8M Payout Over High Failure Rates September 19, 2025 Settlement Reached in Biomet Vanguard Knee Replacement Lawsuit August 14, 2025 Zimmer Biomet Bone Cement Lawsuit Filed Over Failed Knee Replacement July 10, 2025 0 Comments X/TwitterThis 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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: yesterday)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026) Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: 2 days ago)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 3 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
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