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.
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
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.
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.
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.
Recalled Dehumidifier Fires Continue to Cause Property Damage Years Later November 30, 2016 Russell Maas Add Your CommentsFederal safety officials have once again issued a re-announcement for a dehumidifier recall originally issued in 2013, which impacted about 2.5 million dehumidifiers sold under popular brand names like GE, Kenmore and Frigidaire, as additional consumer reports indicate that the devices are overheating and catching fire, which at least $15 million in additional property damage occurring since the devices were originally recalled.ย An updated notice about the Gree dehumidifier recall was posted by the U.S. Consumer Product Safety Commission (CPSC) on November 29, following hundreds of additional consumer reports that indicate the devices are overheating, smoking and catching fire, posing serious burn and fire hazards.Total property damage linked to the recalled dehumidifiers now totals at least $19 million, with the vast majority of that occurring since the original recall was issued, suggesting many of the dangerous and defective dehumidifiers are still in use and their owners likely unaware of the recall.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 original Gree dehumidifier recall was first announced in September 2013, following dozens of reports of the devices overheating and several incidents of the dehumidifiers catching on fire.In January 2014, the recall was expanded after the CPSC and manufacturing company Gree Electric Appliances Inc. recorded a 400% increase in consumer complaints linked to the dehumidifiers overheating and catching on fire. By March 2014, the CPSC reported that the dehumidifiers had caused property damage valued at roughly $4 million.Since the last recall expansion in January 2014, the CPSC and Gree have received at least another 329 reports of fires stemming from overheating dehumidifiers included in the recall. The property damage value has now been estimated at $19 million. The CPSC warns that it is likely that not all of the damage or incidents of fire and overheating has been reported and is urging consumers to stop using and unplug the recalled products immediately.The recall includes roughly 2.5 million 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 announcement.The recalled dehumidifiers were manufactured in China for Gree Electric Appliances. 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 should stop using the recalled dehumidifiers, unplug them, and contact Gree toll-free at 866-853-2802 or visit them online at www.greeusa.com and navigate to the โRecallโ link for information on how to receive a full refund.The warning comes on the heels of another multi-million unit dehumidifier recall announced in early November. The dehumidifier recall included 4 million units manufactured by GD Midea Air Conditioning Equipment Ltd. Of China, which were sold under popular brand names including SunBeam, GE, Honeywell, and Kenmore. The dehumidifiers were recalled following 38 reports of problems where the units overheated, smoked or caught on fire, resulting in nearly $5 million in property damage to date. 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: Dehumidifier, Dehumidifier Recall, Fire, Frigidaire, General Electric, Kenmore, Property DamageMore Lawsuit Stories Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims August 10, 2026 Pressure Cooker Settlement Reached in Lawsuit Over Burns Suffered by Child August 10, 2026 Gold’s Gym Lawsuit Alleges Cable Machine Failed, Causing Traumatic Brain Injury August 10, 2026 0 Comments URLThis 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 Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: today)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims August 10, 2026
Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: today)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)