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 Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs 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.
Super Poligrip Settlements Reached in Some Denture Cream Lawsuits July 28, 2010 Staff Writers Add Your CommentsGlaxoSmithKline has agreed to settle a number of Super Poligrip lawsuits filed by plaintiffs who say they suffered severe and debilitating injuries as a result of zinc poisoning from the denture cream.ย The Super Poligrip settlements were reached with at least one law firm, who filed a motion Tuesday in federal court to establish a fund to satisfy claims involving their clients while the allocation and final disbursement of the monies is finalized. The number of lawsuits over Super Poligrip settled or the amount of money GlaxoSmithKline will pay were not disclosed in the court documents.A few hundred lawsuits have been filed against GlaxoSmithKline and Proctor & Gamble, which manufacturers Fixodent denture cream, in courts throughout the United States by individuals who suffered severe neurological injuries as a result of high amounts of zinc entering their body from the popular over-the-counter products. The Super Poligrip and Fixodent lawsuits allege that the manufacturers failed to inform consumers that the denture cream products contains zinc and failed to warn about the risk or problems that can be caused when too much of the denture adhesive is used.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 AboutโฆSpinal 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 COMPENSATIONDenture cream zinc poisoning can occur when high levels of zinc in the body cause copper depletion, leading to permanent and debilitating neurological problems like neuropathy, numbness, tingling, pain, weakness, loss of sensation, loss of balance, paralysis and difficulty breathing. Although the recommended daily allowance of zinc is 11 mg for men and 8 mg for women, with 40 mg being the maximum amount of zinc that can be safely tolerated, some users of the denture creams have been found to have levels as high as 330 mg per day.All federal lawsuits over Super Poligrip and Fixodent have been consolidated as part of an MDL, or multidistrict litigation, in the U.S. District Court for the Southern District of Florida. A number of state court lawsuits filed in Pennsylvania have also been consolidated into a Mass Tort Program (MTP) in the Philadelphia Court of Common Pleas.Since litigation started, both GlaxoSmithKline and Proctor & Gamble have added zinc warnings to labels and websites for Super Poligrip and Fixodent. Earlier this year, Glaxo announced it was recalling all Super Poligrip products that contained zinc and was replacing them with non-zinc products.The Super Poligrip settlement agreement comes as GlaxoSmithKline has been resolving a number of different outstanding liabilities. Earlier this month it was reported that the company set aside $2.36 billion to settle Avandia lawsuits, Paxil lawsuits and an investigation by the U.S. government. It is unclear whether the costs associated with settling Super Poligrip lawsuits was included in this set aside or whether GlaxoSmithKline has reached similar agreements with other denture cream lawyers. Tags: Denture Adhesive, Denture Cream, Fixodent, GlaxoSmithKline, Proctor and Gamble, Super Poligrip, Zinc Poisoning Image Credit: |More Lawsuit 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 6 Comments calvin August 16, 2012 I am so frustrated with this, I have been fighting this for 3 years. I have filed a lawsuit, and have been miserable for years. I have lost balance and fallen down numerous times. I HAVE HAd 3 mri and nothing, but continue to have problems. Really wish they could figure it out, I am 52 years old, and can no longer work trying to get ssd and ssi but nothing yet,how depressimg Walter August 2, 2012 I was using the polygrip with Zinc in it for years. Ernest April 4, 2011 Was wondering if these products could cause signs of arthritis? My reumitologist can not find any sign of arthritis but I have been diagnosed with chronic pain in both hands andI am now on numerous pain meds. which i can not pass drug screen for employment. susan August 23, 2010 i use fixadent an poligrip serval times a day. i have numbness in my arms had a nerve test but no pinched nerves. saw this ad no i wonder is it zinc exposure. i guess i need to call my doctor and let them test me Cheryl August 7, 2010 My mom called last night. She saw an ad about class action against the Poli-Grip people. She (70rs) has had unexplained pains in her legs now for 3yrs. She has been to plenty of doctors and not one ever told her that she may be suffering from Zinc exposure. I’m shocked that a test like that was never on a test panel. She has been a Poli-Grip user for a number of years (more than 5yrs, I/m sure) She needs help and I and my sisters need answers. june August 7, 2010 I was visiting my daughter in N Mexicoโฆ I had put poligrip on, then we headed out the gate to go shoppingโฆ Suddenly I got a tickle in my throat and could not breatheโฆ I gasped for air, (thought I was dying..) my daughter called 911, they came, I had another attack, The paramedics wanted to take me to the hospital, and I told them that if I had another one, I would Have my daughter take meโฆ then suddenly, I had another attackโฆ.. So I was rushed by ambulance to Prespiterian Hospital in Espanola N. Mโฆ. After a few hours I had another attackโฆ All the attacks started with a tickle in my throat, then my throat would close up, then I could not breathe, I would gasp for air. Some attacks were a minute, some moreโฆ In a 24 hr period I had about 21 attacks, I spent 2 nights in the hospital, no one knew what it wasโฆor what caused it.. I have a huge hospital bill, and I thought it was odd, that every single time, I put on poligrip (one time fix o dent) I would have another attackโฆโฆ.but I thought it was my imagination until I just saw a commericialโฆ go figure?? I donโt know if poligrip was the causeโฆ have you ever heard of symtoms like mine in other Clients?? It has stopped nowโฆ. But I had attacks for about 6 days.. then It went awayโฆ Sure would like to know what caused thisโฆ. And if it was Poligripโฆthen It makes senseโฆ 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 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: 2 days ago)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: 3 days ago)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: 4 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)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 2 days ago)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: 3 days ago)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: 4 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)