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.
Luxor Media Cart Recall Issued After Three Tip-Over DeathsRecalled A/V carts frequently used in classrooms and daycare may tip over under the weight of heavy televisions and equipment. April 14, 2023 Katherine McDaniel Add Your CommentsFederal safety officials have announced a recall of nearly 85,000 plastic and metal media carts, which are commonly used in schools, daycares and recreational facilities, following reports of tip-over accidents that have resulted in the deaths of at least three children.The U.S. Consumer Product Safety Commission (CPSC) announced the Luxor Workspaces Audiovisual Carts recall on April 13, warning the carts can become unstable when loaded with heavy objects, such as box-style televisions or other audio-video equipment.Between 2006 and 2016, the agency is aware of three deaths caused by the unstable carts tipping over on children. The recall notice also indicates there has been at least one other incident involving a child who sustained serious injuries after a television being carried on media cart tipped over, causing the television to fall and land on them.Officials warn that owners should immediately place these carts out of reach of children, should not place anything over 25 pounds on each shelf, and should never allow children climb on the media carts.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 Luxor A/V carts are frequently used in classrooms , daycare centers, places of worship, and other locations. They are intended to hold and transport electronics like televisions, computers, projectors, speakers, and other equipment.The recall impacts three cart base models equipped with three adjustable height shelves. Each of the recalled carts are marked with either the Luxor, Luxor H. Wilson, H. Wilson, Tuffy or Line Leader logo printed on them. The recalled models include:WT42 โTuffyโ plastic cartLP-DUO/TPDUOEQ plastic cartsย W42/AVJ42/SS-AVJ42 metal cartsThe recalled media carts were sold in a variety of colors through multiple websites including Amazon, 123Stores, and Grainger since the early 1980โs for between $125 to $250. About 84,700 of the carts were sold in the U.S., with another estimated 1,650 sold in Canada.Luxor indicates the company will be providing consumers with free repair kits, which will include metal ballast weights that can be installed on the lower shelf to add stability and weight to the cart. To ensure safety further, the manufacturer will also include new warning labels with updated weight limit restrictions for the cart shelves.To request a free repair kit, consumers may visit https://www.luxorworkspaces.com/request-repair-kit, email recall@luxorworkspaces.com, or call Luxor at 800-323-4656 Monday-Friday from 8:30 a.m. to 4:45p.m. CT. Tags: Cart Recall, Child Death, Children, Furniture Recall, Tip OverMore Lawsuit Stories Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026 Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges September 10, 2026 LG Electric Range Lawsuit Alleges Defective Controls Caused House Fire September 10, 2026 0 Comments X/TwitterThis 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 Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)