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.
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
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.
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.
Hydroxycut Liver Failure Lawsuit Filed Following Recall June 16, 2009 AboutLawsuits Add Your CommentsA Wisconsin man has filed a product liability lawsuit alleging that the recently recalled Hydroxycut dietary supplement caused him to suffer jaundice and necrosis of the liver after just over three weeks use.The Hydroxycut lawsuit was filed on June 8 in the U.S. District Court in the Western District of Wisconsin by 28-year-old Marques Parke and his wife, Dawn. The complaint names both Iovate Health Sciences, the manufacturer of the supplement, and Wal-Mart, which sold the Plaintiff Hydroxycut at their Samโs Club Stores.Parke alleges that he suffered serious Hydroxycut liver damage side effects after normal, short-term use of the supplement, which was marketed as a weight-loss aid, fat burner and energy enhancer.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 COMPENSATIONIovate issued a Hydroxycut recall on May 1, 2009, after the FDA identified at least 23 reports of liver damage and one death among users of the product. Although the risk of liver injury was cited as the primary reason for the recall, the FDA also indicated that Hydroxycut was linked to reports of seizures, heart problems and a rare muscle damaging condition known as rhabdomyolysis.After taking Hydroxycut rapid release tablets between March 5, 2008 and March 29, 2008, Parke became ill and went to the emergency room, where he was diagnosed with hepatitis and jaundice. Less than two weeks later he returned to the hospital with worsening symptoms and doctors discovered he had acute hepatitis with necrosis of the liver. He was hospitalized for 11 days.According to the Hydroxycut lawsuit complaint, a liver specialist said the plaintiff โdeveloped hepatoxicity due to the dietary supplement Hydroxycut.โThe case joins a handful of other lawsuits over Hydroxycut filed since the recall last month. More complaints are expected over the coming months as Hydroxycut recall lawyers are investigating potential cases throughout the United States on behalf of individuals who have suffered liver damage or other injuries that may be linked to the dietary supplement. Tags: Dietary Supplement, Hydroxycut, Hydroxycut Recall, Iovate, Liver Damage, Liver Failure, Liver Injury, Rhabdomyolysis Image Credit: |More Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 4 Comments Heather August 26, 2015 It started in 2008. After taking Hydroxycut for over 1 year without no knowledge it would harm my liver, i s when I started getting ill. First I felt weak like my body was closing done on me. Then I turned yellow. They couldn’t find out what was wrong with me. By the exray they ask if I had taken thing, and that’s when I knew it was Hydroxycut. It’s been a stress time for me . I’m getting Var ices .. my spleen is not working, kidneys are now being checked. My life will never be the same.. E. Bandido October 16, 2010 my friends bro is tha 1 who died….they should pay….hey sprewer…what happend to u? CHARLOTTE August 19, 2010 HYDROXYCUT COMPANY NEEDS TO PAY FOR WHAT IT HAS DONE TO PEOPLE AN THEIR FAMILYS. THEY MADE ALOT OF MONEY WITHOUT ANY CONCERNS TO THE FUTURE OF THE BUYERS. D. Sprewer July 6, 2009 I have been under a doctors care since June 2008 because of the side affects of Hydroxycut 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 2 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 3 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 4 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 2 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 4 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)