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.
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
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.
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.
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.
Alloderm Hernia Patch Lawsuits to be Selected for Early Trial Dates in N.J. February 14, 2014 Austin Kirk Add Your CommentsAs several hundred product liability lawsuits continue to move forward in New Jersey state court involving individuals who experienced problems from an Alloderm hernia patch, the parties involved in the litigation are expected to select a small group of cases next week to be prepared for potential bellwether trial that will begin in September 2015.There are currently more than 330 Alloderm lawsuits pending in New Jersey state court, which have been consolidated for coordinated management as part of a Multi-County Litigation, or MCL, before Superior Court Judge Jessica R. Mayer in Middlesex County.All of the complaints involve individuals who suffered complications after receiving the AlloDerm Regenerative Tissue Matrix for hernia surgery or abdominal repair. AlloDerm is manufactured from human tissue harvested from cadavers, which is stripped of the original cells to ensure that recipients do not reject.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 COMPENSATIONWhile Alloderm was originally introduced by LifeCell Corporation in the early 1990s as a skin graft product for use with burn victims during plastic surgery and for certain dental procedures, the lawsuits allege that the manufacturer promoted the patch for hernia surgery and abdominal repairs without adequately researching the application or providing warnings about the need for surgeons to stretch or thin it out before surgery.The complaints all involve similar reports that individuals experienced complications after Alloderm hernia repair, where the patch began to stretch, sag or loosen once implanted. This has been linked to reports of severe abdominal pain, infection, inflammation, injury to nearby organs, adhesion failure, hernia recurrence and other problems.Bellwether Trials for Alloderm LawsuitsLast month, Judge Mayer issued a case management order (PDF) that outlines the process for preparing a small group of cases for early trial dates, which are designed to gauge how juries are likely to respond to certain evidence and testimony that may be similar to what is introduced throughout the litigation.Following the selection of 20 cases for a Bellwether Pool in December, including 10 cases selected by each side, the parties have been directed to further narrow the pool by February 18. Each side will choose four cases each to be eligible for the first bellwether trial, for a total of 8 cases. These claims will then go through case-specific discovery, including the exchange of documents, depositions and other fact discovery, which is to be completed by October 3, 2014.This pool of 8 bellwether Alloderm cases is expected to be further narrowed to a total of four cases by October 17, 2014. Those cases will then go through general causation discovery, including the exchange of expert reports, depositions of expert witnesses and challenges to the admissibility of expert opinions.The first AlloDerm trial is currently scheduled to begin on Monday, September 28, 2015. Such bellwether trials are common in complex medical device litigation, where a large number of cases have been filed against a manufacturer involving similar injuries or factual allegations. The preparation and outcome of such early trial dates may help facilitate further negotiations to reach Alloderm settlements over surgical complications experienced by hundreds of patients.The next case management conference in the New Jersey MCL is currently scheduled for February 26, 2014. Tags: Alloderm, Hernia Mesh, LifeCell, New JerseyMore Hernia Mesh Lawsuit Stories Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict August 17, 2026 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 1 Comments Phil October 7, 2015 Complications from AlloDerm include simple inflammation pain to severe side effects like hernia recurring. malfunction of organs. 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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 Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 2 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026) Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (Posted: 3 days ago)A Kentucky man says his wife died of sepsis and infection complications linked to an Olympus endoscope used during an ERCP procedure.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Colonoscopy Lawsuit Over C. 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Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting August 3, 2026
Boston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (Posted: 2 days ago)Certain Infinion CX spinal cord stimulator leads from Boston Scientific have been recalled after more than 1,000 serious injuries were linked to fractures that may disrupt stimulation and require additional surgery.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJudge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (08/24/2026)
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