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.
Massive Dehumidifier Recall Reannounced After Continuing Reports of Fires May 16, 2014 Russell Maas Add Your CommentsA dehumidifier recall that has already affected more than two million units is being reannounced, as reports of fires connected with the defective dehumidifiers continue to mount, resulting in millions of dollars in property damage nationwide. ย The dehumidifier recall expansion was originally announced by the U.S. Consumer Product Safety Commission (CPSC) in January, and reannounced on May 15. The recall affects units sold under labels including Gree, Kenmore, Frigidaire, Seabreeze and others.The faulty dehumidifiers were originally recalled in September 2013 and the recall was expanded in January 2014.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 CPSC indicates that reports of the units overheating increased by 400% since the original recall, mounting from 119 in September 2013 to 471 reports currently. Reports of fires increased more than 20%, from 46 to 121 reports. Property damage originally recorded at $2.15 million in September is now estimated at nearly $4.5 million. To date no injuries have been reported.The recall includes 20,25, 30, 40, 45, 50, 65, and 70-pint dehumidifiers sold under the brand names Danby, DeโLonghi, Fedders, Fellini, Frigidaire, GE, Gree, Kenmore, Norpole, Premiere, Seabreeze, SoleusAir and SuperClima. The units are white, beige, gray, or black plastic and measure between 19 and 24 inches tall by 13 and 15 inches wide by 9 to 11 inches deep. The brand name and pint capacity are printed on the front of the dehumidifiers and the model numbers and date codes are printed on the back, front, or side of the units. For a full list of recalled brand names, model numbers, and date codes please visit the CPSC recall page.The recalled dehumidifiers were manufactured in China under Gree Electric Appliances where they were imported by various distributing companies and sold at AAFES, HH Gregg, Home Depot, Kmart, Loweโs, Menards, Mills Fleet Farm, Samโs Club, Sears, Walmart and other stores nationwide and online at Amazon.com and Ebay.com in the United States and Canada from January 2005 through August 2013 for between $110 and $400.Customers with affected units should unplug the dehumidifiers immediately and contact Gree at 866-853-2802 or visit them online at www.greeusa.com for information on how to receive a free refund. Customers are encouraged by the CPSC to report any and all adverse events including the products overheating, catching fire and property damage to the manufacturer. 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: Appliance Recall, Dehumidifier, Fire, Home Fire Image Credit: |More Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 0 Comments NameThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: 2 days ago)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 3 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 4 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
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