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.
Core Health & Fitness Exercise Machine Recall Issued After Dozens of Injuries July 13, 2017 Russell Maas Add Your Comments Following more than 50 reports of problems with certain exercise machines distributed throughout the United States, which have resulted in dozens of injuries, a recall has been issued by Core Health & Fitness.ย An Inspiration Cable Cross Over and Dual Adjustable Pulley exercise machine recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on July 12, indicating that at least 48 consumer complaints have bee received, indicating the height adjusting carriage assembly loosened or detached from the machine, falling on users. To date, the CPSC is aware of at least 31 reported injuries resulting in immediate medical attention, including lacerations to the head, neck and shoulder areas that required either stitches or staples. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION The recalled exercise machines may cause serious injury in the event the pulley system’s height adjusting carriage assembly detaches. In the event of the assembly detaching, consumers could be struck on the head by the falling steel assembly. The recall includes five styles of Inspiration Cable Cross Over and Dual Adjustable Pulley machines that are marked with the brand name โInspirationโ, โStar Tracโ or โNautilusโ on the adjustable pulleys. The exercise machines are made of stainless steel and have adjustable pulleys with a single hand adjustment and a high-low cable positioning component. The devices were manufactured in China and the United States by Core Health & Fitness and Land America Health and Fitness of Vancouver, Washington. They were distributed for sale by Core Health & Fitness to Core distributors nationwide from November 2010 through April 2017, and by Unisen distributors from 2001 to 2010 for between $2,700 and $8,400. Recalled machines were primarily sold and installed in fitness centers and gyms across the United States. However, those with home gyms should verify if their exercise system is included within the recall. CPSC officials are asking customers to stop using the recalled exercise machines immediately and to contact Core Health & Fitness at 800-598-8541 or visit them online at www.corehandf.com and navigate to the โRecall Alertโ link for information on how to schedule a free onsite repair. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell 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: Exercise Equipment, Personal Injury More Lawsuit Stories Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL March 26, 2026 Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat March 26, 2026 Genomic Prediction Class Action Lawsuit Claims IVF Testing Is Inaccurate, Unreliable March 26, 2026 0 Comments LinkedInThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (Posted: yesterday) Regeneron and Sanofi-Aventis agree with calls to consolidate all Dupixent cancer lawsuits currently spread throughout the federal court system before one judge. MORE ABOUT: DUPIXENT LAWSUITEnlarged Lymph Nodes Led to Dupixent CTCL Diagnosis, Lawsuit Claims (03/16/2026)Dupixent Mycosis Fungoides Lawsuit Filed Over Failure To Warn About T-Cell Lymphoma Risks (03/09/2026)Dupixent Caused T-Cell Lymphoma or Rapidly Progressed Cancer, Lawsuit Alleges (02/25/2026) Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (Posted: 2 days ago) A group of about 70 Depo-Provera meningioma lawyers have been reappointed to key leadership roles in the litigation, as thousands of women seek compensation for brain tumors they say were caused by the birth control shots. 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Lawsuit Claims Lyft Driver Sexually Assaulted Woman With Her Children in the Back Seat March 26, 2026
Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (Posted: yesterday) Regeneron and Sanofi-Aventis agree with calls to consolidate all Dupixent cancer lawsuits currently spread throughout the federal court system before one judge. MORE ABOUT: DUPIXENT LAWSUITEnlarged Lymph Nodes Led to Dupixent CTCL Diagnosis, Lawsuit Claims (03/16/2026)Dupixent Mycosis Fungoides Lawsuit Filed Over Failure To Warn About T-Cell Lymphoma Risks (03/09/2026)Dupixent Caused T-Cell Lymphoma or Rapidly Progressed Cancer, Lawsuit Alleges (02/25/2026)
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Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (Posted: 3 days ago) Abbott Laboratories faces a lawsuit from a North Carolina woman who says sales representatives repeatedly tried to reprogram a spinal cord stimulator that had already failed due to other problems. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)Boston Scientific Stimulator Problems Resulted in Burning Pain, Shocks From SCS Leads: Lawsuit (03/16/2026)Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (03/10/2026)