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.
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
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.
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.
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.
Home Depot Step Stool Recall Issued After Injury Reports December 12, 2012 Russell Maas Add Your CommentsAbout 20,000 extendable stepstool ladders sold exclusively at Home Depot have been recalled, after multiple reports indicate that the inner and side walls may collapse suddenly, potentially causing serious injuries for consumers.ย A Wing Enterprise Inc. Switch-it Stepladder/Stepstools recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on December 11, after the manufacturer received at least nine injury reports by customers.The reports indicate that the inner rails separated from the outer rails, causing the user to fall. The severity of injuries has ranged from minor scrapes and contusions to a broken collar bone. Because the ladder extends to six feet high, the defect could pose a substantial risk for consumers who may fall, potentially landing on top of the dismantled aluminum pieces.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 recalled ladders were manufactured in China by Suzhou Zhongchuang Aluminum Products Co. LTD. and imported by Wing Enterprise Inc., of Springville, Utah.The Switch-it Type 1A stepladder/stepstools extend from a 2 foot stepstool to a 6 foot ladder, with a weight capacity of 300 pounds. The ladders are silver and have C-channel outer rails with orange rocker-type locks on each side to hold the outer rails to the inner rails. The words “Switch-it by Little Giant” appear on the top of the ladder in orange and white writing. Recalled Switch-it Type 1A models have part number “15124” on the notice label attached to the back of the outer rails and the following “date stamps” are located on the orange locks: 10622S,10623S, 10624S, 10721S, and 10722S.The recalled stepstool ladders were sold exclusively at Home Depot stores and online at Homedepot.com from August 2012 to October 2012 for about $88.The CPSC recommends that consumers immediately stop using the recalled stepstool ladders and contact Wing Enterprise at (855) 595-3378 for a free replacement of the front outer section. Consumers can also visit the company’s website at www.littlegiantladders.com/switch-it-recall for more information. 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: Home Depot, Step Stool RecallMore Lawsuit Stories FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk November 9, 2026 Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL November 9, 2026 Teen Social Media Use Linked to Depression, Anxiety and Cyberbullying: Study November 9, 2026 0 Comments InstagramThis 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 FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk (Posted: today)Federal regulators are requiring all GLP-1 medications to carry new label warnings indicating the side effects could put patients at risk of sudden and permanent vision loss.MORE ABOUT: OZEMPIC LAWSUITOzempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (10/30/2026)GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026) Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL (Posted: today)Individuals involved in Boston Scientific SCS implant lawsuits have submitted a Master Complaint that would help streamline future filing.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (11/02/2026)Abbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026) Apple AirTags Allowed Abusive Husband to Stalk, Control Wife, Lawsuit Alleges (Posted: 3 days ago)A woman’s lawsuit claims her husband used an Apple AirTag bluetooth tracking device to stalk and abuse her.MORE ABOUT: APPLE AIRTAG LAWSUITLawsuit Claims Defective Apple AirTag Safety Features Allowed Domestic Violence Stalking (10/26/2026)Lawsuit Alleges Apple AirTag Tracker Used to Monitor Womanโs Location (10/14/2026)Apple AirTag Stalking Lawsuits Consolidated in Northern District of California (10/08/2026)
FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk November 9, 2026
Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL November 9, 2026
FDA Requires New Vision Loss Warnings for Ozempic, Wegovy and Other GLP-1s Over NAION Risk (Posted: today)Federal regulators are requiring all GLP-1 medications to carry new label warnings indicating the side effects could put patients at risk of sudden and permanent vision loss.MORE ABOUT: OZEMPIC LAWSUITOzempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (10/30/2026)GLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)
Consolidated Lawsuit Over Boston Scientific Spinal Cord Stimulator Problems Filed in MDL (Posted: today)Individuals involved in Boston Scientific SCS implant lawsuits have submitted a Master Complaint that would help streamline future filing.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (11/02/2026)Abbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)
Apple AirTags Allowed Abusive Husband to Stalk, Control Wife, Lawsuit Alleges (Posted: 3 days ago)A woman’s lawsuit claims her husband used an Apple AirTag bluetooth tracking device to stalk and abuse her.MORE ABOUT: APPLE AIRTAG LAWSUITLawsuit Claims Defective Apple AirTag Safety Features Allowed Domestic Violence Stalking (10/26/2026)Lawsuit Alleges Apple AirTag Tracker Used to Monitor Womanโs Location (10/14/2026)Apple AirTag Stalking Lawsuits Consolidated in Northern District of California (10/08/2026)