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.
Wireless Light Switch Recall Issued Due to Risk of Fires October 22, 2009 AboutLawsuits Add Your CommentsAbout 1.3 million Handy Switch wireless light switches have been recalled due to reports that they may overheat or cause a fire.The U.S. Consumer Product Safety Commission (CPSC) announced the Idea Village Products Corp.โs Handy Switch wireless light switch recall on Wednesday. The recall came after the company received 14 reports of the wireless light switches overheating, including nine cases where the switch burst into flames.The Handy Switch receiver, which plugs into a wall outlet, is a white, plastic wireless remote light switch with a blue electroluminescent nightlight. The model number KS-080 will be printed on the back of the receiver.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 Handy Switch was sold by mass merchandisers, drug store chains, television infomercials and online across the U.S. from March 2007 through July 2009. The receivers were made in China.The CPSC recommends that consumers immediately unplug and stop using all Handy Switch wireless light switches and contact Idea Village for information on free remedy options. Anyone who experiences an incident or injury due to the devices should contact the CPSC at https://www.cpsc.gov/cgibin/incident.aspx. Tags: Fire, Wireless Light Switch Recall Image Credit: |More Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 11 Comments Karen April 19, 2026 I have been using this for many years. Love it. I just saw this article. Is there still replacements available. Please! Bun March 19, 2015 If you have this get rid of it. Mine caused a fire. The light overheated, bubbled and turned into a flame. Luckily I came home from work just in time to put it out but only after it had caused a carpet burn and smoke in my office. You can only imagine the horror of coming home opening the door of the house and seeing it filled with smoke and the smoke alarms going off. I traced the smoke to my office where there was a bright flame burning on the floor where the handy switch was located. Luckily I had a fire extinguisher handy. Had a come home an hour or even 30 minutes later who knew what further damage it would have caused! Tianna December 28, 2014 Just saw this after trying to see if it was available on Amazon. Guess I will be looking for another brand as well. nikki April 24, 2014 wow..didnt know about this..odd mine just went out tonite, thought it was lite bulb, then noticed the nite lite out, figure maybe the battery in the wall switch needs replacing..now i see this recall..not going to get replacement..just rather purchase something else..not going to deal with this company …glad i saw this Stephanie November 29, 2013 I’ve had my handy switch for years and use it regularly with my youngest who is afraid of the dark. Never noticed any problems with it. However recently it finally failed me and the plug no longer works at all. I would like a new one as our house has no upstairs hallway light switch at the bottom of the steps. dave April 10, 2012 I got 4 units with G3706 labels on the back. Are these affected too? Noticed with all that the night light works just the opposite of how it should. In other words it is lit when the lamp is on and goes out once the switch is turned off Jeff February 11, 2012 Mailed defective unit back in December, still waiting for replacement. Herman September 20, 2010 I had a fire caused by the handy switch I was lucky i don’t lose the whole house but the repairs and smoke damage totaled almost ten thousand dollars. Joe March 2, 2010 I had no problems with my plug. But dont risk it…get the free replacement handyswitchrecall.com George February 14, 2010 I’ve been using the these switches for over 9 months to a year. Found them handy. Am alarmed now that they are ‘blowing out’ my bulbs. Suddenly a big poof and the bulbs are burnt, not the blue base. Has anyone had this problem and did’nt connect it to a faulty KS 080? Richard October 24, 2009 I have been using my handy switches for over a year now and don’t want to give them up… What are the real dangers and what are my options?????? 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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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)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) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine 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)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 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)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)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)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine 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)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 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)