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.
Chlorpyrifos Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
Ram ProMaster Recall Issued Due to Vehicle Fire Risks From Defective Radiator FansManufacturer’s investigation determined that premature wear within the fan system and insufficient fuse protections could increase the risk of Ram ProMaster vehicle fires. October 28, 2025 Darian Hauf Add Your CommentsThe U.S. National Highway Safety Administration (NHTSA) announced a Ram ProMaster recall on October 24, warning that nearly 300,000 vehicles may have a flawed radiator fan design that could increase the risk of an electrical short circuit. The radiator fan is located under the hood and helps keep the engine cool by pulling air through the radiator to lower coolant temperatures, which is the liquid that prevents the engine from overheating.The fan operates through an electrical circuit that controls when the fan turns on and off. If that circuit overheats or malfunctions, the fan motor can generate excessive heat, potentially sparking an engine compartment fire and increasing the risk of property damage or serious injury.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know About…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAccording to the recall report (PDF), Ram first became aware of the issue on July 3, after its FCA US Technical Safety and Regulatory Compliance organization detected a trend of fires originating from the cooling fan module in certain Ram ProMaster vehicles.The manufacturer reported at least 39 customer assistance records and field reports involving the cooling fan module, though no accidents or injuries have been linked to the issue so far.The investigation continued over the following months, until the root cause was found to be premature bearing wear, meaning parts inside the fan wore out sooner than they should, combined with inadequate fuse protection on the 400W fan circuit, which failed to prevent the fan from overheating.As a result of the findings, FCA US, Ram’s parent company, decided to conduct a voluntary safety recall (PDF) of 291,664 model year 2018 through 2026 Ram ProMaster vehicles on October 16.Customers will begin receiving interim notification letters explaining the safety risk on November 20. Additional letters will be sent once the final remedy is available. FCA US, also known as Chrysler, has assigned recall number 67C to this action. Customers may contact Chrysler customer service at 800-853-1403 or the manufacturer’s contact for the recall, Emily Smith, by email at emily.c.smith@dot.gov.Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-275-9171), or go to www.nhtsa.gov.Sign up for more safety and legal news that could affect you or your family. Tags: FCA, Radiator, Radiator Fan, Ram, Ram ProMaster, Ram Promaster Van Image Credit: rafaelnlins / Shutterstock.com Written By: Darian HaufConsumer Safety & Recall News WriterDarian Hauf is a consumer safety writer at AboutLawsuits.com, where she covers product recalls, public health alerts, and regulatory updates from agencies like the FDA and CPSC. She contributes research and reporting support on emerging safety concerns affecting households and consumers nationwide.More Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 0 CommentsInstagramThis 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: yesterday)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026) Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems Patients are developing serious infections after colonoscopy and ERCP procedures, as concerns grow that reusable endoscopes may not be fully… Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit Women who experienced infection, chronic inflammation, implant instability or other complications after internal bra mesh procedures are now questioning whether… Young People and Gambling: Why Men Are Disproportionately Affected by Sports Betting Addiction As legal sports betting expands nationwide, research and emerging lawsuits suggest that young men face disproportionate risks from mobile sportsbook… The ‘Can’t Feel My Feet’ Symptom Doctors See in Nitrous Oxide Nerve Injury Nitrous oxide injury lawsuits are emerging as medical evidence links recreational use of the gas to nerve damage that can… Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts Plastic surgeons are sounding the alarm over the rising use of mesh-based “internal bra” procedures, warning that the materials may… Sudden Ozempic Blindness Reports Raise Concerns Over NAION Side Effects An increasing number of Ozempic and Mounjaro users are reporting sudden, irreversible vision loss from NAION side effects, prompting new… GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director Former Becton Dickinson safety officer Dr. Hooman Noorchashm warns that the company’s GalaFLEX mesh is being used off-label in breast… Sports Betting Corruption and Addiction Concerns Highlighted By Recent MLB, NBA Player Indictments Federal indictments against MLB and NBA players reveal how legalized sports betting has blurred the line between competition and addiction,… Amazon Fire Pit Safety Warnings Issued to Customers Amid Burn Injury Lawsuits Recall notices are being sent to Amazon customers who purchased tabletop fire pits linked to severe burn injuries, as lawsuits… Internal Bra Mesh Failure Stories Highlight Risk of Pain, Infections and Other Problems Women are sharing alarming reports of pain, infections, and reconstruction failures caused by internal bra mesh implants like GalaFLEX, as… Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful… Dupixent Cancer Risks Outlined in User Stories, as Evidence Mounts of T-Cell Lymphoma Link Dupixent users are coming forward with accounts of devastating cancer diagnoses, saying the popular eczema drug masked early warning signs…
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: yesterday)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems Patients are developing serious infections after colonoscopy and ERCP procedures, as concerns grow that reusable endoscopes may not be fully…
Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit Women who experienced infection, chronic inflammation, implant instability or other complications after internal bra mesh procedures are now questioning whether…
Young People and Gambling: Why Men Are Disproportionately Affected by Sports Betting Addiction As legal sports betting expands nationwide, research and emerging lawsuits suggest that young men face disproportionate risks from mobile sportsbook…
The ‘Can’t Feel My Feet’ Symptom Doctors See in Nitrous Oxide Nerve Injury Nitrous oxide injury lawsuits are emerging as medical evidence links recreational use of the gas to nerve damage that can…
Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts Plastic surgeons are sounding the alarm over the rising use of mesh-based “internal bra” procedures, warning that the materials may…
Sudden Ozempic Blindness Reports Raise Concerns Over NAION Side Effects An increasing number of Ozempic and Mounjaro users are reporting sudden, irreversible vision loss from NAION side effects, prompting new…
GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director Former Becton Dickinson safety officer Dr. Hooman Noorchashm warns that the company’s GalaFLEX mesh is being used off-label in breast…
Sports Betting Corruption and Addiction Concerns Highlighted By Recent MLB, NBA Player Indictments Federal indictments against MLB and NBA players reveal how legalized sports betting has blurred the line between competition and addiction,…
Amazon Fire Pit Safety Warnings Issued to Customers Amid Burn Injury Lawsuits Recall notices are being sent to Amazon customers who purchased tabletop fire pits linked to severe burn injuries, as lawsuits…
Internal Bra Mesh Failure Stories Highlight Risk of Pain, Infections and Other Problems Women are sharing alarming reports of pain, infections, and reconstruction failures caused by internal bra mesh implants like GalaFLEX, as…
Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful…
Dupixent Cancer Risks Outlined in User Stories, as Evidence Mounts of T-Cell Lymphoma Link Dupixent users are coming forward with accounts of devastating cancer diagnoses, saying the popular eczema drug masked early warning signs…