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.
Thalidomide Side Effects Were Hidden By Manufacturer: Report May 16, 2016 Irvin Jackson Add Your Comments The makers of the controversialย morning sickness drug Thalidomide, which has been linked to thousands of birth defects worldwide, appears to have intentionally misled investigators and the public decades ago in an effort to hide the side effects associated with the controversial drug, according to German officials.ย In a report released by the German state of North-Rhine Westphalia (NRW), investigators from the University of Muenster indicate that the drug manufacturer Gruenenthal gave the medical and scientific community false information about the potential Thalidomide side effects, kept knowledge of problems associated with the drug a secret, and delayed efforts to remove the drug from the market as long as possible. The activities happened decades ago, when the side effects of thalidomide were first suspected, according to the investigation, which was reported by Reuters. 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 Thalidomide was first released as a morning sickness drug in 1957. Four years later, it was removed from the market after it was determined that the thalidomide caused major birth defects when used during pregnancy. It was the first product that established medications could cross the placental barrier and cause harm to a fetus. It is estimated that between 10,000 and 20,000 children were born worldwide with birth defects from thalidomide. Itโs impact was limited in the United States because the FDA denied the drug approval, saying that it needed to be more thoroughly tested. However, the drug was given to doctors in the U.S. during its clinical testing phase and it is unclear how many children it affected. Thalidomide is now sold under the brand name Thalomid and is used for the treatment of multiple myeloma. In 2012, Gruenenthal officials formally apologized to those who continue to suffer birth defects due to the drug’s side effects and dedicated a statue to thalidomide victims in Stolberg, Germany. Following the apology over the thalidomide birth defects, many victims told various media outlets that the action was insulting and did little those who were born with life-long health problems caused by the drugโs side effects. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin 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: Birth Defects, Pregnancy, Thalidomide 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 1 Comments Paul November 17, 2016 Just need to know why it now haven’t had any one contact me over my birth defect 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 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)