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.
Walmart Trampoline Recall Expanded Due to Defective Netting January 31, 2013 Russell Maas Add Your CommentsAn additional 120,000 trampolines have been recalled by Walmart, due to problems with the enclosure netting, which may break and pose a fall hazard for children.ย A Sportspower BouncePro 14′ Trampoline recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on January 30, after at least 9 reports were received, including five cases that involved broken bones, back, neck injuries and contusions that were suffered when the black enclosure netting broke. The trampolines were sold exclusively at Walmart.The recalled Sportspower BouncePro 14′ Trampolines are surrounded by a 6 feet high black tetlon netting around the perimeter designed to contain individuals bouncing on the trampoline. The recall involves trampolines with model number TR-1686-TPR and UPC code 687064045552 or 687064042100 printed on the product box. “Sportspower BouncePro 14′ Trampoline” is printed on a plate located on the leg of the trampoline frame.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 COMPENSATIONThe trampolines were manufactured in China by SportsPower Ltd., of Hong Kong and sold exclusively at Walmart stores nationwide from February 2009 through March 2011 for about $300.The recall is an expansion of an earlier Walmart trampoline recall issued in May 2012, which originally consisted of 92.000 trampolines. In that case, models with a brown tetlon netting were linked to at least 11 reports of injuries.At-home trampolines have been widely recognized as dangerous products, especially for children. The American Academy of Pediatrics recommends that trampolines never be purchased for home use, and that parents should not to allow their children to play on trampolines at the homes of others. The American Medical Association has also urged parents not to allow children to play on trampolines.A recent study by Rhode Island Hospital researchers found that an average of 88,563 children are taken to the emergency room every year for a trampoline injury, with 95% involving injuries that happen on home trampolines. The study was presented at a 2007 American Academy of Pediatrics annual meeting and showed a significant increase in trampoline injuries from previous years.The CPSC recommends that consumers stop using the trampolines immediately and contact SportsPower at (888) 965-0565 to receive a replacement enclosure netting. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Children, Trampoline, Trampoline Injury, WalmartMore Lawsuit Stories Fire Pit Burn Injury Lawsuit Alleges Defective Amazon Product Engulfed Child in Flames July 10, 2026 States Seek $1.4T in Social Media Addiction Damages From Facebook, Instagram July 10, 2026 Crest Toothpaste Contains Harsh Mouth-Damaging Chemicals: Lawsuit July 10, 2026 0 Comments PhoneThis 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 Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: yesterday)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026) Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: 2 days ago)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026) Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 3 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
Suboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: yesterday)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)
Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: 2 days ago)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 3 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)