Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures
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.
Recalled Hope Chest Caused Death of Two Children, Years After Warnings January 21, 2014 Irvin Jackson Add Your Comments Ten years ago, millions of cedar hope chests were recalled following the deaths of more than half a dozen children. The suffocation deaths of two more children this month in one of those same chests ย highlights a major problem with product recalls in the United States: the inability to make certain dangerous products are removed from circulation. On January 12, 8-year-old Lexi Munroe and 7-year-old Sean Munroe, of Franklin, Massachusetts, apparently climbed into a Lane Furniture Company Hope Chest and became trapped inside, suffocating. The chest, and 12 million like it, were recalled in 1996, after similar reports involving children who climbed inside and then suffocated. A dangerous design feature causes the chests to latch shut automatically when closed, and there is no way to open it from the inside. 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 Constructed between 1912 to 1987, the U.S. Consumer Product Safety Commission (CPSC) and the manufacturer announced the cedar chest recall in 1996, following at least six deaths. The recall was announced again in 2000, following another death and reports of at least two more children who were trapped inside, but able to escape without catastrophic injury. Despite all those warnings, the chest remained in the Munroe family home, and federal safety regulators are concerned that the item may be found in homes for years to come, as the hope chests are often handed down from one family to the next. Kids in Danger, a nonprofit organization focused on child-safe products, estimates that only about 30% of all items that are recalled are actually removed from consumers’ homes. That means that as many as 8.4 million of the Lane cedar chests are likely still in consumers’ homes. The organization seeks to get more manufacturers to get it right the first time, instead of relying on recalls to detect faulty products when it is often too late. Experts say that in many cases, most consumers are completely unaware of recalls involving products in their homes, even when those recalls are massive and repeated several times. Some product safety advocates have pushed for more proactive notification systems that require manufacturers to contact known purchasers of products that have been recalled. This practice is often used in the automotive industry. The initial Lane cedar chest recall affected all of the company’s cedar chests manufactured before 1987. The company initially replaced the locks on the chests, which latch automatically when closed. The website for the replacement locks is still up, but it is unclear whether the company still replaces the latches. If not, CPSC officials urge everyone to check their homes for these chests and to just throw them away if they cannot get the lock replaced, and not pass them on to others or continue to use them. Consumers can check to see if their chest is one of those recalled by closing the chest lid without depressing the locking button and then trying to open the lid without touching the button. If the lid opens, the chest is fine. If the lid is latched, throw the chest away. Consumers with questions can call the CPSC Hotline at (800) 638-2772. 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: Children, Childrens Furniture Recall Image Credit: | More Lawsuit Stories Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures March 11, 2026 UPF Lawsuit Blames Food Industry for 14-Year-Oldโs Type 2 Diabetes Diagnosis March 11, 2026 Lawsuit Alleges Amazon Heating Pad Failed To Shut Off, Causing Severe Burn Injury March 11, 2026 0 Comments CommentsThis 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 Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: today) 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. Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: yesterday) 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) Dupixent Mycosis Fungoides Lawsuit Filed Over Failure To Warn About T-Cell Lymphoma Risks (Posted: 2 days ago) A Georgia couple’s lawsuit claims the makers of Dupixent failed to provide adequate warnings about the risk of mycosis fungoides, a type of T-cell lymphoma. MORE ABOUT: DUPIXENT LAWSUITDupixent Caused T-Cell Lymphoma or Rapidly Progressed Cancer, Lawsuit Alleges (02/25/2026)MDL Sought for Dupixent Lymphoma Lawsuits Filed in Federal Courts Nationwide (02/19/2026)Lawsuit Claims Dupixent for Atopic Dermatitis, Eczema Treatment Caused CTCL (02/10/2026)
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures March 11, 2026
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: today) 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.
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: yesterday) 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)
Dupixent Mycosis Fungoides Lawsuit Filed Over Failure To Warn About T-Cell Lymphoma Risks (Posted: 2 days ago) A Georgia couple’s lawsuit claims the makers of Dupixent failed to provide adequate warnings about the risk of mycosis fungoides, a type of T-cell lymphoma. MORE ABOUT: DUPIXENT LAWSUITDupixent Caused T-Cell Lymphoma or Rapidly Progressed Cancer, Lawsuit Alleges (02/25/2026)MDL Sought for Dupixent Lymphoma Lawsuits Filed in Federal Courts Nationwide (02/19/2026)Lawsuit Claims Dupixent for Atopic Dermatitis, Eczema Treatment Caused CTCL (02/10/2026)