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.
Fentanyl Patch Wrongful Death Lawsuit Alleges Design Defect February 2, 2012 Staff Writers Add Your Comments A wrongful death lawsuit has been filed against ALZA Corporation by the family of a Utah woman who died in 2010, after using one of the company’s fentanyl pain patches.ย The fentanyl patch lawsuit was filed by the family of Janine Ward late last month in Salt Lake City’s 3rd District Court. The complaint names ALZA Corporation, a subsidiary of Johnson & Johnson, as a defendant. According to the claim, the fentanyl patch, also known as a transdermal patch, was defectively designed and leaked fentanyl gel when applied to Janine Ward’s skin. 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 Johnson & Johnson, ALZA’s parent company, first developed the first pain patch as the Duragesic patch in 1994. Since it was introduced, the fentanyl patch has been plagued by manufactured problems and a number of wrongful death lawsuits filed by families of individuals who overdosed on fentanyl. Fentanyl is a painkiller about 100 times more powerful than morphine, and poses a severe risk of overdose and death if the gel contained within the patch leaks out and comes into direct contact with the skin of patient or caregiver. The gel in the patch is supposed to be contained and delivered in a regulated fashion through a membrane placed on the skin. However, over the last several years the FDA has received hundreds of reports of fentanyl overdoses and deaths associated with the use of fentanyl pain patches. In many of the cases, too much of the fentanyl was delivered through the skin due to manufacturing defects. There have been a number of fentanyl patch recalls due to defective manufacturing. That is what Ward’s family says killed her in May 2010 after using one of the patches. A toxicology report found she had lethal levels of fentanyl in her blood at the time of death. The lawsuit claims that ALZA used a reservoir design that failed to protect Ward from a potential overdose. According to the complaint, the death may have been avoided if ALZA had used a much safer matrix design; technology the plaintiffs say was known to the company. Tags: Duragesic, Fentanyl, Fentanyl Overdose, Fentanyl Patch, Utah, Wrongful Death More Fentanyl Patch Lawsuit Stories U.S. Drug Overdose Deaths Increased 30% to All-Time High in 2020: CDC July 20, 2021 Synthetic Opioid Deaths Increased More Than 1,000% In Recent Years: CDC February 12, 2021 FDA Announces New Risk Mitigation Strategy To Address Opioid Crisis December 28, 2020 0 Comments CompanyThis 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 Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) 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: yesterday) 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) Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (Posted: 4 days ago) In a joint statement, plaintiffs and defendants in AngioDynamics port catheter lawsuits have laid guidelines for what types of cases should be selected to serve as potential bellwether trials. MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Blood Clot Results in Lawsuit Against Device Manufacturer (02/04/2026)SmartPort Infection Lawsuit Alleges AngioDynamics Catheter Defects Forced Surgical Removal (01/30/2026)Severe Sepsis Infection Leads to Vortex Port Catheter Wrongful Death Lawsuit (01/12/2026)
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: today) 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: yesterday) 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)
Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (Posted: 4 days ago) In a joint statement, plaintiffs and defendants in AngioDynamics port catheter lawsuits have laid guidelines for what types of cases should be selected to serve as potential bellwether trials. MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Blood Clot Results in Lawsuit Against Device Manufacturer (02/04/2026)SmartPort Infection Lawsuit Alleges AngioDynamics Catheter Defects Forced Surgical Removal (01/30/2026)Severe Sepsis Infection Leads to Vortex Port Catheter Wrongful Death Lawsuit (01/12/2026)