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.
Hernia Mesh “Completely Dissolved”, According to Lawsuit Over Ethicon Physiomesh August 29, 2017 Irvin Jackson Add Your CommentsProblems with Ethicon Physiomesh allegedy caused an Oregon woman to suffer painful complications following hernia repair, according to a product liability lawsuit filed after the hernia mesh totally dissolved inside her wound.The complaint (PDF) was filed by Melinda Rall in the U.S. District Court for the District of Oregon on August 22, naming Johnson & Johnson and its Ethicon subsidiary as defendants.Rall underwent hernia repair surgery in September 2015, which involved the placement of a 25cm by 35cm Ethicon Physiomesh patch. However, the next month she was readmitted for a CT guided asperation of an anterior abdominal wall seroma. A year later, she was again hospitalized, but this time the surgeon found that the hernia mesh had become adhered to multiple loops of her small bowel. The adhesions were freed in a two to three hour surgical procedure, parts of the Physiomesh were removed, and additional mesh was implanted to fill in the gapsHernia 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 COMPENSATIONIn February 2017, Rall was again hospitalized for pain, recurrent incisional hernia and other problems.“The Physiomesh implanted in Plaintiff appeared to have disintegrated or completely dissolved in the area of the hernia,” Rall’s lawsuit indicates. “The Physiomesh implanted in Plaintiff was also found to be disrupted with bowel bulging through. Plaintiff’s Physiomesh was removed from the surface of the underlying bowel.”The lawsuit indicates that Ethicon and Johnson & Johnson had a duty to adequately design, test, and manufacture the mesh to ensure that it was safe and effective before being placed on the market. The complaint claims the manufacturers failed in that duty.The case joins a growing number ofย Ethicon Physiomesh lawsuitsย filed by individuals nationwide who have experienced complications following laparoscopic hernia repair in recent years.Given the similar questions of fact and law presented in casesย ย pending throughout the federal court system, the U.S. Judicial Panel on Multidistrict Litigation (JPML) decided last month to establish coordinated pretrial proceedings, centralizing all cases before U.S. District Judge Richard Story in the Northern District of Georgia to reduce duplicative discovery, avoid contradictory pretrial rulings and to serve the convenience of the parties, witnesses and the courts.Rall’s case will be transferred to the federal multidistrict litigation (MDL), which currently includes nearly 100 other claims. However, asย hernia mesh lawyersย continue to review and file additional cases in the coming weeks and months, it is expected that several thousand complaints will ultimately be included in the litigation. 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: Ethicon, Hernia, Hernia Mesh, Johnson & Johnson, PhysiomeshMore Hernia Mesh Lawsuit Stories Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial August 5, 2026 Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting August 3, 2026 Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection July 27, 2026 5 Comments Ernesto September 6, 2017 That surgery ruind my life,I lost my job that I was there for almost 11 years I could go back because of the pain ,I couldn’t get a job because of the reason I was dismissed,led to my divorce to because of financial problems I still have pain every time I over do it at work if I would never got that surgery I know my life would of been the same because I still feel like I use to feel withaut the surgery I’m not trying to get a free ticket because money can’t give me back my old life back,Ijust want these blue collar basterds to get a taste of their own medicine.it took me 3 years to get use to living like this Wanda September 4, 2017 I’m haveing the same problems with my mesh from my hernia surgery back in dec of 2015 I’m having surgery again on the twenty second of this month. Judith September 1, 2017 Omg! I wonder if that’s what happened to me? I have had severe, debilitating pain since a femoral hernia repair! I asked a surgeon to see if maybe a stitch or something was on my nerve, or maybe my body was rejecting the mesh? …only to find out, after they went back in laproacopically, there was no mesh! This nerve damage has COMPLETELY altered my life!? Judith September 1, 2017 Omg! I wonder if that’s what happened to me? I have had severe, debilitating pain since a femoral hernia repair! I asked a surgeon to see if maybe a stitch or something was on my nerve, or maybe my body was rejecting the mesh? …only to find out, after they were t back in laproacopically, there was no mesh! This nerve damage has COMPLETELY altered my life!? gerald August 31, 2017 All white collar criminals that put in( foreign material) mesh of any kind should spend time in prison.Have the same experience along with those that manufacture (foreign material)mesh to them.C.R.Bard also. 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 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 Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: today)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026) Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine 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)
Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting August 3, 2026
Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection July 27, 2026
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: today)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)
Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026)
Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine 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)