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.
Target Dresser Recall Issued After Tip-Overs Onto Children September 15, 2017 Russell Maas Add Your CommentsMore than 175,000 four-drawer dressers sold exclusively by Target have been recalled, after the manufacturer received at least a dozen reports of the heavy furniture pieces tipping over on young children, posing a risk of serious and potentially life-threatening injury. ย The Target dresser recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on September 13, due to the potential tip-over hazard, which has already resulted in injuries for at least two three-year old children.According to the CPSC, the dressers are unstable if they are not anchored to a wall, posing a serious risk in homes throughout the U.S. To date, the agenccy has received reports of the pieces both tipping over and collapsing.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 COMPENSATIONIncluded in the recall are Target Room Essentials 4-drawer dressers, which measure 41 7/8 inches tall by 31 ยฝ inches wide by 15 11/16 inches deep. The dressers were sold in the color black with model number 249-05-0103, espresso with model number 249-05-0106, and maple with model number 249-05-0109. The model numbers of the recalled furniture pieces can be found on the productโs packaging.The recalled dressers were manufactured in Denmark and distributed for sale at Target stores nationwide, and online at Target.com, from January 2013 through April 2016, for about $118.The CPSC estimates about 175,000 units were distributed for sale throughout the United States, and an additional 3,000 units were sold in Canada.Customers are being asked to stop using the dressers drawers immediately if they are not properly anchored to the wall, and to place the dresser in an area that children cannot access.The recalled Target dressers can be returned to any Target store for a full refund. For further questions or concerns regarding the recall, consumers may contact Target at 800-440-0680 or visit them online at www.Target.com and navigate to the โRecallsโ tab at the bottom of the page.Earlier this month, Walmart was also subject to a dresser recall that included an estimated 1.6 million Ameriwood Mainstays 4-drawer dressers recalled 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.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. 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, TargetMore Lawsuit Stories Study Finds Dose Response Link Between Alcohol and Pancreatic Cancer June 26, 2026 Federal Lawmakers Seek Paraquat Ban Amid Parkinson’s Disease Lawsuits and Settlements June 26, 2026 Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 June 25, 2026 0 Comments EmailThis 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 Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (Posted: yesterday)A federal judge has scheduled the first Dupixent lawsuit MDL initial case management conference for October 1, 2026.MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026) Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: 2 days ago)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026) AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (Posted: 3 days ago)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)
Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 June 25, 2026
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