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.
Cybex Arm Curl Exercise Machine Recall Issued After Multiple Injury Reports August 26, 2015 Russell Maas Add Your Comments Following more than 100 reports of problems with Cybex arm curl machines, including at least a dozen injuries, the manufacturer has issued a recall due to the risk that the handles may suddenly break while exercising. The Cybex arm curl exercise machine recall was announced by the U.S. Consumer Product Safety Commission on August 25, impacting more than 4,400 pieces of equipment sold to gyms throughout the country. Reports suggest that the swivel handle may break off from the frame, posing a serious injury risk. At least 12 incidents have been reported where exercisers suffered an injury when the arm curl handle detached and hit the user in the face. One case involved the loss of vision in one eye as a result of the injury. 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 arm curl machines are designed to allow the consumer to sit down on an adjustable seat and select an amount of weight resistance. The user then grabs the swivel handles to perform a curl motion toward them to exercise their biceps and arm muscles. If the swivel handle on the arm curl exercise machine detaches from the frame while the user is applying force to the resistance, it can result in a risk of serious and permanent injury. As a result of the defect, the swivel handle may be projected toward the users face, potentially resulting in bruising, laceration or fractures. With the manufacturer receiving 108 incident reports from only 4,400 machines sold to customers, it is likely that these machines will eventually break over time and constant use, the CPSC warns. Due to the machines being a popular fitness club and gym machine that is used frequently, the CPSC is asking all consumers to stop using the machines immediately. The recall includes the Cybex International arm curl machines with model names VR2, VR2TA, Eagle, and VR3. The model name can be located on the top of the machine and the serial number can be found on the frame tube of the weight stack by the base of the unit. For a full list of recalled model numbers and serial numbers please visit www.cybexintl.com. The arm curl machines were manufactured in the United States under Cybex International Inc. of Medway, Massachusetts where they were sold at through Cybex or its distributors directly to gyms from November 1996 through October 2008 for between $3,700 and $4,200. Consumers are being asked to stop using the fitness equipment immediately and contact Cybex International at 888-678-3846 or visit them at www.cybexintl.com and navigate to the โSupportโ link for a free repair kit. Cybex announced that they are contacting customers on file directly to warn of the potential dangers and repair process. 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, Vision Loss More Lawsuit Stories 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates April 7, 2026 Lawsuit Claims Roblox Showed Reckless Disregard for Child Safety April 7, 2026 Kenmore Dehumidifier Lawsuit Alleges Device Ignited, Caused More Than $150,000 in Damages April 7, 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 10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates (Posted: today) A federal judge has selected 10 hair relaxer lawsuits to serve as potential bellwether trials after altering the selection process to eliminate non-representative cases. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (04/01/2026)Hair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026) High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: yesterday) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026) Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 4 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Kenmore Dehumidifier Lawsuit Alleges Device Ignited, Caused More Than $150,000 in Damages April 7, 2026
10 Hair Relaxer Lawsuits Selected by Court for Early Trial Dates (Posted: today) A federal judge has selected 10 hair relaxer lawsuits to serve as potential bellwether trials after altering the selection process to eliminate non-representative cases. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (04/01/2026)Hair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)
High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: yesterday) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 4 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)