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.
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 Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope July 14, 2026 SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection July 14, 2026 Instant Pot Safety Lawsuit Claims Defective Pressure Cooker Caused Burn Injuries July 14, 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 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 Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: today)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026) Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: yesterday)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026) First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 4 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)
Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: today)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)
Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: yesterday)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)
First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 4 days ago)The first Covidien hernia mesh bellwether trial begins on Monday in Massachusetts federal court involving claims that the Symbotex mesh is defectively designed.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (06/10/2026)Bard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)