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.
Bard Ventralex Lawsuit Claims Hernia Mesh Incompatible With Human Tissue January 4, 2018 Irvin Jackson Add Your Comments Davol, Inc. and C.R. Bard face another product liability lawsuit over complications associated with their hernia mesh products, alleging that that the Bard Ventralex mesh is not compatible with human tissue. In a complaint (PDF) in the U.S. District Court for the Southern District of Mississippi on January 2, Patrick Dove alleges that the manufacturers sold a defective product that was not suitable for use during hernia repair surgery. Dove under went hernia surgery in March 2014, at which time an 8 cm circular Bard Ventralex patch was implanted in his body. However, complications and severe pain with the hernia mesh led to him requiring additional revision surgery in June 2017. Hernia Mesh Lawsuits Did 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 More SEE IF YOU QUALIFY FOR COMPENSATION Hernia Mesh Lawsuits Did 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 More SEE IF YOU QUALIFY FOR COMPENSATION The Bard Ventralex is a self-expanding patch that contains two layers of polypropylene mesh, which are stitched together with polytetrafluorethylene monofilament to an expanded polytetrafluorethylene sheet. The lawsuit raises allegations similar to those presented in a growing number of other product liability complaints, indicating that the layers have a tendency to delaminate, resulting in “folding, shriveling, curling up on edges and generally causing a separation of layers of the patch.” “The Bard Ventralex mesh was actually made of materials, which are biologically incompatible with human tissue and react negatively and sometimes dangerously with a large number of those on whom it is used,” Dove’s lawsuit states. “Defendant knew or should have known that their product was unreasonably harmful.” Dove’s lawsuit presents claims of negligence, design defect, manufacturing defect and breach of warranty. The case is part of a growing number of hernia mesh lawsuits being filed in courts nationwide against manufacturers of various devices introduced in recent years, which have been linked to reports of painful and debilitating complications. In addition to a number of other Bard Ventralex lawsuits, a particularly large number of Atrium C-Qur lawsuits and Ethicon Physiomesh lawsuits, leading to the federal court system to establish centralized pre-trial proceedings for all litigation involving those two products. As product liability lawyers continue to review and file additional cases over Bard Ventralex problems, it is possible that another multidistrict litigation (MDL) will be established for all claims filed against C.R. Bard and it’s Davol subsidiary. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin 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: Atrium C-Qur, Atrium Medical, C. R. Bard, Davol, Ethicon, Hernia, Hernia Mesh, Physiomesh, Ventralex Image Credit: | More Hernia Mesh Lawsuit Stories Covidien ProGrip Hernia Mesh Lawsuit Joins Over 2,200 Similar Claims in MDL January 9, 2026 Covidien Symbotex Mesh Lawsuit Reset For Trial in July 2026 November 24, 2025 Feb. 2026 Trial for Covidien Hernia Mesh Lawsuit Canceled by MDL Judge November 5, 2025 0 Comments FacebookThis 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 Lawyers Call for Hair Relaxer Cancer Lawsuit To Be Set for Trial (Posted: today) Ahead of a case management conference this week, hair relaxer cancer lawsuit lawyers have asked a federal judge to set a date for the first bellwether trial. MORE ABOUT: HAIR RELAXER LAWSUITPresentations on How Hair Relaxers Cause Cancer Will Be Heard by MDL Judge This Week (01/05/2026)Hair Relaxer Manufacturers Push for Evidence Many Plaintiffs Did Not Likely Keep (12/10/2025)Hair Relaxer Lawsuit MDL Status Hearings Scheduled Throughout 2026 (11/13/2025) Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: yesterday) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025) Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 2 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020)
Lawyers Call for Hair Relaxer Cancer Lawsuit To Be Set for Trial (Posted: today) Ahead of a case management conference this week, hair relaxer cancer lawsuit lawyers have asked a federal judge to set a date for the first bellwether trial. MORE ABOUT: HAIR RELAXER LAWSUITPresentations on How Hair Relaxers Cause Cancer Will Be Heard by MDL Judge This Week (01/05/2026)Hair Relaxer Manufacturers Push for Evidence Many Plaintiffs Did Not Likely Keep (12/10/2025)Hair Relaxer Lawsuit MDL Status Hearings Scheduled Throughout 2026 (11/13/2025)
Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: yesterday) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025)
Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 2 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020)