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.
Walmart Dresser Recall Issued Over Tip-Over Risk September 7, 2017 Russell Maas Add Your CommentsMore than 1.6 million chests of drawers sold primarily at Walmart have been recalled, due since the dressers do not comply with furniture tip-over requirements, and may pose a risk of serious injury for small children.The Walmart Ameriwood Home dresser recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on September 6, after at least one report was received where one of the four-drawer chests tipped over onto a four-year-old, entrapping and injuring the child.The four-drawer chests are being recalled due to their failure to comply with the performance requirements of industry standards, which are intended to reduce injuries and deaths of children from hazards associated with the tip over of free-standing clothing storage units, such as chests, door chests and dressers, over 30 inches in height.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 COMPENSATIONThese standards were developed due to the growing concerns of furniture tip-over injuries recorded across the U.S. in recent years.According to CPSC data,ย furniture and TV tip-over accidents have caused 430 deaths over the last 13 yearsย and account for roughly 38,000 emergency rooms visits annually. The commission warns that at least one child dies every two weeks and another child is injured every 24 minutes in the U.S. from heavy furniture or televisions tipping over.Several dresser and chest recalls have been issued in recent years with the largest being the IKEA recallย in June 2016, which pulled more than 35 million child and adult chests and dressers from the market. The recall came after at least 17 injuries and three deaths were linked to its MALM dressers.Children are inherently more susceptible to tip-over accidents from climbing and reaching for items at the top of dressers, or television stands, whether it is for a remote, gaming equipment or toys. The CPSC recommends that parents never leave items desirable to children on dressers and other top heavy furniture that would entice the child to try and climb or reach for them.1.6 Million Mainstays Chests of Drawers RecalledThe CPSC initiated the latest recall after receiving a report from the manufacturer that a four-year-old child was injured after a four-drawer chest of drawers tipped over on the child, posing a suffocation, trauma, and serious injury hazard.Included in the recall are Mainstays four-drawer chests of drawers that are equipped with plaster drawer slides and a single decorative pull on each of the four drawers. The chests are made of a composite wood and were sold in the colors alder, black forest, white, weathered oak, walnut and ruby red. The chests measure 40 5/16 inches high by 27 11/16 inches wide by 14 11/16 inches deep and are marked with model numbers 5412012WP, 5412301WP, 5412328WP, 5412015WY, 5412301WY, 5412012PCOM, 5412015PCOM, 5412026PCOM, 5412213PCOM, 5412214PCOM, 5412301PCOM, 5412317PCOM, and 5412328PCOM, which are printed on the instruction manual.The Walmart Mainstays dressers were manufactured in the U.S. and Canada by Ameriwood Home of Tiffin, Ohio. They were distributed for sale throughout the U.S. to Walmart stores and other retail stores as well as online through various retailers from April 2009 through May 2016 for about $60.The CPSC announced an estimated 1.6 million units were sold throughout the United States and an additional 1,000 units were distributed for sale in Canada.Customers with recalled chests of drawers are being asked to stop using them immediately if they are not properly anchored to the wall, and to move them into an area where children cannot access them. Customers should contact Ameriwood at 877-222-7460 or visit them online at www.Ameriwood.com and navigate to the โSupportโ tab for information on how to receive a free repair kit that includes a wall anchoring device and wider feet for the base of the unit. 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: Children, Furniture Recall, WalmartMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 0 Comments CommentsThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard 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)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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