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.
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.
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.
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
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.
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.
Parietex Progrip Mesh Lawsuit Filed Over Hernia Repair Complications July 6, 2017 Irvin Jackson Add Your CommentsAccording to allegations raised in a product liability lawsuit brought by a Louisiana man, the Covidien Parietx Progrip hernia mesh is unreasonably dangerous and defective, causing him to suffer painful complications following hernia repair.The complaint (PDF) was filed late last month by Jason Bruce in the U.S. District Court for the Eastern District of Louisiana, naming C.R. Bard, Davol, Inc, Medtronic Inc. and Covidien as defendants.Bruce indicates that Parietex Progrip Mesh was used during to repair a right inguinal hernia in June 2016. However, as a result of problems with the design of the hernia mesh, Bruce indicates that he developed severe pain and swelling, as well as problems walking, which led to the need for additional surgery to have the hernia mesh patch removed.Hernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONHernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATION“The product has numerous defects that create a high risk of unreasonable and dangerous injuries and side effects with severe permanent adverse health consequences including that the material in the Product abrades tissues adversely affecting patient health and regularly fail to perform the purpose of its implantation such that the patient requires repair and/or removal of the Product and repeated treatment and surgery,” the lawsuit states. “Prior to the time that the Product was implanted in Plaintiff, Defendants were aware of numerous defects in the Product. Despite being aware of the numerous defects and unreasonable ricks in the Product, Defendants designed, manufactured, marketed, and distributed the Product with the intent they would be implanted in patients.”According to the lawsuit, the manufacturers were aware of numerous reports of problems with Parietex Progrip Mesh long before Bruce’s hernia repair. However, they never adequately informed the medical community or patients of those injuries and the potential problems with their product, the lawsuit claims.Bruce’s complaint is one of a growing number of hernia mesh lawsuits being filed against various mesh manufacturers, alleging that serious design problems were discovered after thousands of people had defective mesh implanted in their body.In addition to Covidien Parietex Progrip Mesh lawsuits, similar allegation have been raised in Ethicon Physiomesh lawsuits and Atrium C-Qur lawsuits as well.Bruce presents claims of construction or composition defect, inadequate warning, design defect, breach of warranty, and redhibition, seeking compensatory and punitive damages. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin 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: C. R. Bard, Covidien, Davol, Hernia, Hernia Mesh, Medtronic, Parietex Progrip Image Credit: |More Hernia Mesh Lawsuit Stories Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications June 10, 2026 Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities June 3, 2026 Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026 5 Comments Michael January 31, 2023 I had Perietex Progrip inguinal mesh implanted four years ago and have dealt with severe pain and inflammation since I woke from surgery. Since then, I reinjured myself, been out of work for two years, had numerous, nerve blocks, bilateral nerve ablations, six nerves cut, five veins in the groin tied off and months of physical therapy. After all of this, I cannot find an attorney to take my case for having a permanent implant that cannot be removed. It has destroyed my life and livelihood. Rick December 18, 2021 I had surgery in 2006 and cannot find the specific Parietex used. The operative report on says it was parietex but no other details. Grant September 3, 2017 I had the Parietex Composite placed into my abdomen in late 2008 after a hernia repair. Almost immediately after surgery I knew something was not right. At my 2 week post surgical appointment I had a huge racquet ball sized lump in my right armpit. I was given some antibiotics and brushed off as if it were nothing. A few days later the test came back positive for MRSA. Lump finally went away after three rounds of antibiotics 2 of which were bactrim. Even though the lump went away my surgical wound never completely healed. It was mostly closed except for three holes along the incision (top, middle, and bottom). These were tunneling oozing infected wounds and they were positive for MRSA as well. These tunneling wounds went deep back into my abdomen and required cleaning and packing of gauze strip into the tunnels twice a day with horrid smells and extreem almost unbearable pain at times. To make a long story short the surgeon was an ass and a master at blowing me off as if these problems were caused by me. So after a couple months of the runaround I just stopped seeing him because he wasn’t helping. Over the next 1 1/2 years I seen several different doctors at hospitals and wound clinics and they were all stumped as to the cause of this wound not healing. I was sent on so many tests and studies (MRI, Cat, Fistulagrams, sonogram xray etc….) to try to ascertain the cause of the wound but to no avail. Finally in 2011 I found a doc who refused to just pass the buck and was commited to getting to the answer . While doing a full open exploratory abdominal procedure it was discovered, in the very lowest part of my wound wadded and balled up was the entire piece of mesh that was installed in the upper abdomen in 2008. The mesh was infected and rotting in my gut for over 2 years. The tunneling wounds that had never healed had to be cleaned and derided. When it was over the full open wound was as big around as a large grapefruit and as deep as a racquet ball. I was on a wound vac post surgery for over 3 months while the gaping hole in my stomach healed. The complications healthwise I’ve had since the initial placing of the mesh have been horrendous. The pain and discomfort is so awful I have a hard time doing anything that requires any amount of strength or stamina. After the removal of the mesh in 2011 I have never been able to return to work. I have applied for SS disability twice since 2011 only to be denied both times after the appeal process. I have uncontrollable diarrhea every day as well as enormous amounts of gas that’s horrid. I can barely eat a meal due to the nerve damage and gastroparesis I now suffer from as result of all the abdominal surgeries. The gerd and nerve damage cause me to vomit sometimes multiple times a day. I’m so anemic I have to be infused with iron twice a month. This has truly been an awful chapter in my life. Since I couldn’t go back to work of course I lost my health insurance and any shred of dignity I had left because now I have to ask someone for everything because I have no means of support. SS tells me because I’m under 50 they can’t approve my benefits that I paid In to the system for by having a job my entire life since I was 16. Now with both denials and the time that had passed they tell me that even though I had earned way over the amount if work credits needed to get my ss disability that the rule is you have to have earned work credits sometime in the 5 years previous to any application for benefits and now even though I’ve applied twice and been denied that now I’m beyond the 5 years for having a work credit so now I’m not eligible for any of the benefits I paid in for my entire life. At best they say I could maybe get a few hundred in SSI but that’s only if they approve that. I have been screaming since 2008 about the defective Parietex that caused me all of this harm but could never find an attorney willing to persue it. I’ve been very depressed at times and wanted to check out. Sometimes that sounds like the best plan but for some reason I hang on hoping maybe someday ill get some justice just maybe. -G- shawn July 13, 2017 Sept.15 -2014 had this mesh put in across whole lower groin and belly button against my will. Since that time I have suffered great pain and disability. Up to present. 7-2017 the mesh that has had all the attention has. Been pysiomesh complaints up to now. Glad to see this partiicular parietex mesh implant is finally part of the expossure to defect and life changing trauma. sue July 7, 2017 This is what I have and nothing but pain since implant. This will be yet another one that becomes a recognized medical device failure in Australia after thousands of people have it implanted. 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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 Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (Posted: yesterday)A tentative Depo-Provera lawsuit settlement has been announced, vacating the start of the first bellwether trial while details are finalized.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026)Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026) Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 4 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 5 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)
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