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.
Heparin Overdose Kills 2-Year Old Transplant Survivor April 7, 2010 Staff Writers Add Your CommentsA two-year-old girl appears to have died of a heparin overdose in an Omaha hospital after being admitted to treat an infection. This tragedy is the latest in a string of infant overdoses involving the blood thinner.Almariah Duque, a 23 month old girl from Dallas, was born with a birth defect and had survived a transplant of her small intestines, pancreas and liver in December, according to a CNN report. However, despite surviving the surgeries, Duque died at the Nebraska Medical Center on Wednesday after being given too strong a dose of the blood thinner Heparin.Duque was given the drug, an anticoagulant, to prevent blood clotting. The hospital has apologized to Duque’s parents, and have agreed to pay medical and funeral expenses.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 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 COMPENSATIONThe little girl’s death, which is still under investigation by hospital officials, is one of a number of incidents in recent years where infants overdosed on heparin due to preventable human errors.In October 2006, three premature infants died from a fatal heparin overdose at Methodist Hospital in Indianapolis, when the hospital used adult dosage vials of Baxter heparin instead of pediatric dosage vials. Following that incident, Baxter Healthcare Corp. sent a warning letter to healthcare workers stressing that they should read labels on the heparin vials with care to prevent such mistakes.Another similar medication mistake was made in November 2007 at Cedars-Sinai Medical Center in Los Angeles, where babies were given the adult doses of the blood thinner, instead of the pediatric version. Although Baxter had agreed prior to this incident to change the labels for their pediatric heparin to avoid confusion, they did not issue a heparin recall for the existing stock of the drug that remained with hospitals.Actor Dennis Quaid’s newborn twins were among the babies that were given 1,000 times the normal dosage. Quaid later filed a product liability lawsuit against Baxter, the makers of heparin, alleging that the product was unreasonably dangerous because the company packaged adult and pediatric versions of the blood thinner in vials of the same size, with nearly identical blue backgrounds, making it difficult to tell them apart.In July 2008, 14 premature babies at a Texas hospital were given incorrect heparin doses, resulting in several deaths. That incident was attributed to a pharmacy dosing error, which resulted in babies in the neonatal intensive care unit being given much higher concentrations of blood thinner than they were prescribed. Tags: Baxter, Birth Defect, Blood Thinner, Heparin, Heparin Recall, Infection, Nebraska, Product Liability Image Credit: |More Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Stretch August 21, 2011 Grade A stuff. I’m unquestonaibly in your debt. 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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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a man’s 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: 2 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: 3 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)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a man’s 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: 2 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: 3 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)