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.
Paxil Lawsuit over Birth Defects Remanded to Pennsylvania State Court October 2, 2013 Austin Kirk Add Your CommentsA federal judge has agreed to remand a Paxil birth defect lawsuit back to Pennsylvania state court, following an attempt by the manufacturer to have the case removed to the federal court system two years after the complaint was first filed. ย The product liability lawsuit was first brought by Theresa Powell and her daughter, Madison Powell, in the Philadelphia Court of Common please in June 2011, alleging that the mothers use of Paxil during pregnancy caused the child to develop birth defects.Following the original filing of the complaint in Pennsylvania’s Mass Tort Program, which was established for all Paxil lawsuits involving birth defects, GlaxoSmithKline removed the case to the federal court system based on the argument that Powell is a citizen of California. However, that initial removal was reversed in December 2011, when a U.S. District Judge granted the plaintiffs’ request to remand the case back to state court and held that the drug maker was a citizen of the state of Pennsylvania, which would prevent Glaxo from seeking federal jurisdiction over a lawsuit filed in Pennsylvania state court.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDispute regarding the proper venue of Paxil birth defect lawsuits has been on-going in a number of cases filed in Pennsylvania’s state court system, as Glaxo has been attempting to remove the cases to federal court since it is perceived as a more favorable location for the drug maker, based on the belief that juries will be less likely to award substantial compensation to children left with severe birth defects from the drug maker’s failure to warn about the pregnancy risks with Paxil.Following the 2011 remand of the Powell case back to Philadelphia’s Mass Torts Program, the parties engaged in substantial discovery and the lawsuit was scheduled for trial begin on October 21, 2013. However, Glaxo filed a second Notice of Removal on June 26, 2013, after another group of birth defect lawsuits against the drug maker were successfully kept in the federal court system when the U.S. Court of Appeals for the Third Circuit ruled that Glaxo is a citizen of the State of Delaware.In a Memorandum (PDF) issued in the Powell case on September 26, U.S. District Judge Michael Baylson granted plaintiff’s Motion to Remand (PDF) and returned the case back to Pennsylvania state court.Judge Baylson concluded that the second removal was untimely because it occurred more than a year after the action commenced, that the Third Circuit decision does not impact the prior decision to remand this case and that all doubts about whether a case should be sent back to state court should be resolved in favor of remand, which has now been ordered in this case.Paxil Birth Defect LawsuitsThe dispute over whether the Powell case should move forward in state or federal court comes after GlaxoSmithKline has previously agreed to pay several billion dollars in Paxil settlements to families of children who suffered birth defects or malformations. The continued attempts to avoid state court jurisdiction appears to be part of the drug maker’s effort to reduce the value of outstanding cases.Paxilย (paroxetine) is a selective serotonin reuptake inhibitor (SSRI) prescribed to treat depression. Approved in 1992, it has become one of the most commonly prescribed drugs in the United States, generating sales of about $1 billion a year.In December 2005, the FDA issued an alert in the United States about the risk of birth defects from Paxil, after studies showed the drug could increase the risk of the heart defects when taken during the first three months of pregnancy. At that time, the agency also required GlaxoSmithKline to update the warning label in this country to include information about the pregnancy risks with Paxil.The company has faced hundreds of Paxil lawsuits in the United States, which were brought on behalf of children who suffered various birth defects and malformations, such asย persistent pulmonary hypertension in newborns (PPHN)ย and other health problems. The complaints alleged that Glaxo purposefully hid test results that would have revealed the risks associated with use of Paxil during pregnancy and misled doctors.In October 2009, a Pennsylvania jury awarded the family of a three year old child $2.5 million inย compensation for birth defects from Paxil, following the first trial in the country. In 2010, it was reported that GlaxoSmithKline set aside $2.4 billion toย settle Paxil birth defect lawsuits. Tags: Birth Defect, GlaxoSmithKline, Paxil, Paxil Birth Defect, Pennsylvania Image Credit: |More Zoloft Lawsuit Stories Intestinal Bleeding Risk Linked To SSRIs Combined With NSAIDS: Study November 2, 2021 SSRI Antidepressants Linked To Slight Increased Risk of Childhood Diabetes: Study September 23, 2020 Higher Risk Of Recurring Brain Bleeds Linked to SSRI Antidepressant Side Effects September 9, 2020 0 Comments URLThis 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 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: yesterday)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 2 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge 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) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 3 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard 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)
Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: yesterday)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: 2 days ago)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge 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)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 3 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard 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)