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.
IKEA Children’s Lamp Recall Issued After Infant Strangles in Crib December 12, 2013 Russell Maas Add Your CommentsFollowing the death of a 16-month old child who strangled on the cord of a wall-mounted lamp, a recall has been issued for nearly 23 million lamps sold exclusively at IKEA. ย The IKEA wall mounted lamp recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on December 11, following the infant death and at least one other report that another toddler became tangled in the 7 foot long power cord. In both incidents the infants were able to pull the cord into their crib, causing the strangulation hazard.The CPSC has determined that the lamps pose a serious strangulation hazard due to the long electrical cord used to run a source of power to the wall outlets. The risks are that children can pull the cords into the crib and become entangled in them.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 IKEA childrenโs SMILA-series wall mounted lamps recall includes eight different designs with the following names and model numbers; Blue Star STJARNA model with article numbers 501.944.49 or 500.108.79; Yellow Moon MANE model with article numbers 701.944.48 or 700.108.40; Pink Flower BLOMMA model with article numbers 901.944.47 or 000.979.50; White Flower Blomma model with article number 300-746-50; Rd Heart HJARTA model with article numbers 202.256.59 or 801.993.13; Green Bug BAGGE model with article numbers 101.944.46 or 700.728.71; Blue Seashell SNACKA model with article number 400-982.50; and Orange Seahorse SJOHAST model with article number 900-982-43.The affected lamps measure about 11 inches high by 11 inches wide and have a 7-foot electrical cord with an in-line power switch that connects to a 25-watt light bulb. The lamps have the model name and article number printed on the inside of the lamp near the bulb and on the lampโs packaging.The products were manufactured in the United States, Lithuania, and China where they were sold exclusively at IKEA stores nationwide as well as in IKEAโs catalog and online at ikea-usa.com from July 1999 through May 2013 for between $10 and $13 dollars. IKEA estimates to have sold 2.9 million in the U.S., 1.1 million in Canada, and the rest were sold worldwide.The CPSC is calling for customers to stop using the recalled lamps immediately and contact IKEA at (888) 966-4532 or visit them online at www.ikea-usa.com and navigate to the recall link to receive a free repair kit. IKEA has announced plans to provide customers with self-adhesive fasteners for attaching the lamps cord to the wall and a safety instructions manual. IKEA is urging customers to not use the lamps again until the repair kit has been installed. 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, Ikea, Infant Death, Strangulation Image Credit: |More Lawsuit Stories Cuisinart Grill Brush Class Action Lawsuit Claims Recalled Products Contained Dangerous Defects July 15, 2026 Tampax Tampon Lawsuit Claims Feminine Hygiene Products Contain PFAS, Heavy Metals July 15, 2026 Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope 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: yesterday)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: 2 days ago)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: 5 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)
Cuisinart Grill Brush Class Action Lawsuit Claims Recalled Products Contained Dangerous Defects July 15, 2026
Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: yesterday)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)
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First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (Posted: 5 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)