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.
Gas Line Valves Recalled Due to Fire and Explosion Hazard December 12, 2012 Irvin Jackson Add Your CommentsAbout 163,000 shut-off gas valves have been recalled due to manufacturing defects, which could pose a potential risk of fires or gas explosions. The Fu San Machinery gas valve recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on December 11, impacting seven brands of valves used in both homes and businesses.The CPSC warns that the low lead ball valves and shut-off gas valves affected by the recall can crack. Although there have been no reports of injuries or incidents associated with the defect, the recalled gas line valves could cause a gas leak, fire and possibly an explosion.Learn More AboutBurn Injury LawsuitsInfo about lawsuits for burn injuries from fires and gas explosions caused by another’s negligence.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutBurn Injury LawsuitsInfo about lawsuits for burn injuries from fires and gas explosions caused by another’s negligence.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDefective Valves Sold to Seven Different DistributorsThe recall affects seven brands of sweat and threaded low lead nall valve/shut-off gas valves manufactured by Fu San Machinery Co. Ltd., of Taiwan.The valves were sold to seven different distributors in the United States, including Aqualine, AY McDonald, FNW, Hodes Co., Legend, Leonard Valve and Mueller. A complete list of valve dimensions and model numbers is available in the recall announcement.The recalled valves are used in flammable gas piping systems. They are brass and have a date code of 1103 through 1112, with the first two digits representing the year and the last two digits representing the month. The date code is under the valve handle, the pipe size is on the body of the valve, and the Fu San logo and an “O” designating them as low lead valves are located on the neck. The valves were sold nationwide from April 2011 through January 2012 for $13 to $20.The CPSC recommends that consumers who have the recalled gas valves should turn off the gas supply until a replacement gas valve has been installed by a professional.Danville Sales, representing Fu San Machinery, is compensating consumers $300 for having to replace and return the valve. To receive the refund, the affected valves must be returned to the Danville Sales Office for Fu San Machinery along with a photo of the valve installed in the gas line before it was removed. The date code must be shown on the valve as well as the address and details of the location where it was installed.The valve, photo, information and the customer’s name and address should be sent to Danville Sales Office for Fu San Machinery, 1101 N. Kings Hwy, Cherry Hill, New Jersey 08034. Consumers with questions can call (855)779-9200, or visit the company’s website at www.fsvalve.com.tw and click on the Safety Recall Notice button.According to the National Fire Protection Association (NFPA), natural gas and propane gas home fires between 2000 and 2004 resulted in 66 deaths and over 400 injuries. On average, NFPA estimates that there are about 2,410 natural gas home fires and 1,390 propane gas fires every year. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Fire, Gas Explosion, Gas LeakMore Burn Injury Lawsuit Stories Breville Pressure Cooker Recall Issued After Reports of Burns December 23, 2015 E-Cigarette Burns from Battery Explosion Left Florida Man In Medically-Induced Coma December 2, 2015 Keurig Coffee Maker Recall Announced After Dozens of Burn Injuries Reported December 23, 2014 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: yesterday)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 2 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Woman’s CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 3 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamics’ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Woman’s Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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