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.
Alloderm Hernia Mesh Lawsuits Moving Forward in N.J. State Court July 3, 2012 Austin Kirk Add Your CommentsThe number of lawsuits filed over the AlloDerm hernia patch continue to increase as the litigation moves forward in New Jersey state court.According to a case list issued last week, there are currently more than 150 AlloDerm lawsuits that are centralized for pretrial proceedings in the Superior Court for Middlesex County, and a case management conference is scheduled for next week, on July 10.The complaints have been filed on behalf of individuals throughout the United States who suffered serious and painful complications from the AlloDerm patch, after it was used for a hernia repair or abdominal reconstructive surgery.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 COMPENSATIONOriginally introduced in the early 1990s, the AlloDerm Regenerative Tissue Matrix is a skin graft product that is manufactured from tissue harvested from cadavers, which is stripped of the original cells to ensure that recipients do not reject it.While AlloDerm was originally introduced by LifeCell Corporation for use with burn victims during plastic surgery and for dental procedures, the manufacturer has also promoted the patch for hernia surgery and abdominal repairs.According to allegations raised in the AlloDerm hernia repair lawsuits, when the patch is used in the abdomen it must be “pre-stretched” to keep it from expanding over time. However, LifeCell allegedly failed to adequately warn doctors about this risk, which could cause abdominal deformity, pain, disability and hernia recurrence.LifeCell initiated a silent recall of AlloDerm for use in hernia repair surgeries, according to the master complaint filed in New Jersey. LifeCell no longer advertises, promotes or markets AlloDerm for use during hernia or abdominal surgery, and plaintiffs allege that the product was never safe or suitable for such uses due to its elasticity.Although AlloDerm had been on the market since about 1992, LifeCell did not inform surgeons that it could stretch by up to 50% until 2008. In May 2011, the company instructed surgeons to suture AlloDerm under significant tension in order to reduce its ability to stretch as much as possible.AlloDerm was the first commercial product sold by LifeCell, and grew to generate more than $167 million in revenue for the company in 2007. It has been used in more than one million grafts and implants. For hernia repair, LifeCell now promotes the use of Strattice Reconstructive Tissue Matrix, a surgical mesh made using pig skin. Tags: Alloderm, Hernia, Hernia Mesh, LifeCell, New Jersey Image Credit: |More Hernia Mesh Lawsuit Stories Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications June 10, 2026 Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities June 3, 2026 Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026 3 Comments Lydia September 10, 2016 I had Strattice 8×8 cut and breast tissue removed for Strattice to be layered under the nipple. NO IMPLANT was used. Dr was trying to correct lumpectomy defect. My breast is bleeding around the areola and turning purple. Dr said he is stunned. LifeCell said it is not the Strattis. I do not wish sepsis Jermaine January 28, 2016 Multiple wound dehiscence, infections, and recurrences resulting in complete abdominal reconstruction. Strattice mesh buckled in on itself in a total of 4 surgeries. Will explain in further detail upon request Val August 15, 2013 Breast Aug 4/30/13 silicone implants with Strattice ,My plastics insisted for the issues of capsular contraction an bottoming, needed more Said he couldn\\\\\\\’t do surgery without the use of Strattice ,,Long story short my breast opened around the incision area twice ,In the hospital with sepsis,, after almost 4 months of serous fluid and chances of losing my implants completely ,he wanta to take out the Strattice More surgery!!!.. implants and hospital i been out over 27000$ So that\\\\\\\’s my experience with the\\\\\\\” latest greatest \\\\\\\” X/TwitterThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 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: 3 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) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 4 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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