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.
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.
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.
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.
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.
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.
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.
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.
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.
Food Poisoning Prevention Rules Issued by FDA Target Imports, Produce November 16, 2015 Russell Maas Add Your Comments Government food safety officials have released a series of new rules that are designed to regulate imported foods and produce, in an attempt to reduce the risk of food poisoning outbreaks in the U.S.ย Last week, the FDA announced three new major food safety rules to catch and prevent foodborne illness outbreaks before products reach the United States. The new rules establish enforceable safety standards for produce farms and food importers to adopt science-based contamination prevention methods, food sampling and testing requirements, and to allow for third party auditors to certify facilities are meeting FDA food safety requirements. Do You Know about… SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The FDA released the new rules amid a highly active year in the U.S. involving imported foodborne illness outbreaks. FDA Deputy Commissioner Michael Taylor cited the recent multi-state Salmonella outbreak caused by imported cucumbers, which has killed four and hospitalized over 150 consumers. According to the U.S. Centers for Disease Control and Prevention (CDC), there are an estimated 48 million people sickened each year from food poisoning. An estimated one out of six Americans get sick each year, almost 130,000 are hospitalized, and about 3,000 people die annually from all foodborne related illnesses. “The FDA is working with partners across the government and industry to prevent foodborne outbreaks,” Taylor said in the press release. “The rules will help better protect consumers from foodborne illness and strengthen their confidence that modern preventive practices are in place, no matter where in the world the food is produced.” The three rules released in the FDAโs statement on Friday include the Produce Safety Rule, the Foreign Supplier Verification Program, and the Accredited Third-Party Certification rule. The Produce Safety Rule requires importers to establish science-based standards for growing, harvesting, packing, and shipping. Included in these rules are standards on water quality, employee health and hygiene, wild and domesticated animals, compost and manure samples, and equipment, tools, and buildings. The list of rules and standards included in the Produce Safety Rule are designed to help remove and mitigate any or all possible threats of dangerous bacteria contaminating imported produce. The Foreign Supplier Verification Program will require food importers to verify foreign suppliers are producing food that meets the U.S. safety standards. It requires importers to conduct audits of the supplierโs facility including sampling and testing of food as well as review of the supplierโs relevant food safety records. The finalized rule on Accredited Third-Party Certification establishes a program for the accreditation of third-party certifications auditors to conduct food safety audits and verify foreign food facilities are following acceptable FDA food safety requirements. This rule allows the FDA to require specific food imported to be accompanied by a third-party certification ensuring it is safe to enter the U.S. All of the new rules are the result of the Food Safety Modernization Act (FSMA). The ultimate goal is to use the nation’s technology and experience to help farmers and food businesses successfully produce safe foods for import. According to the FDA, these are three of seven major rules that will shape the new FSMA guidelines. FDA officials say it is important for there to be strict guidelines and that these rules systematically strengthen the food safety system and better protect the public from imported goods. The United Stated Department of Agriculture (USDA) estimated that in 2013, 19% of the food supplied in the U.S. was imported. Additionally, 52% of the fresh fruits were imported along with 22% of the countryโs vegetables. The rules were not solely established by the governing agencies. The final rules were established after holding conferences and meetings with farmers, stakeholders, and taking consideration into public comments. Taylor added in the press release that the agency is confident the new rules will help prevent disease from entering the U.S., but said the success of the rules are contingent on funding from the Obama Administration’s 2016 budget request. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Food Poisoning More Lawsuit Stories Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week March 12, 2026 Enfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects March 12, 2026 Stainless Steel Apple Watch Bandโ Lawsuit Filed Over Burn Injury Risks March 12, 2026 0 Comments EmailThis 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 Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026) Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026) Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)
Enfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects March 12, 2026
Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026)
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026)
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)