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.
Massive Kidde Fire Extinguisher Recall Issued After Failures, Death November 3, 2017 Russell Maas Add Your CommentsMore than 40 million Kidde fire extinguishers are being recalled, following more than 400 reports of the devices failing to work in a fire emergency, which may have resulted in at least 16 injuries and one fatality.The Kidde fire extinguisher recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on November 2, due problems that may cause millions of units distributed nationwide to fail, limit activation or experience a nozzle detachment, each of which may pose a serious risk for consumers and property owners.Among reports of the Kidde fire extinguisher problems are at least 91 incidents that resulted in property damage,ย and 16 injuries from smoke inhalation or burns that occurred when consumers could not activate the extinguishers. The agency is also aware of one death that occurred in 2014, following a car fire where the extinguisher failed to operate.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 recalled fire extinguishers are equipped with a plastic handle that can become clogged or require excessive force to discharge. This may cause the fire extinguisher to fail to activate during an emergency. The extinguishersโ nozzles may also detach with enough force to pose an impact hazard to users.Included in the recall are both Kidde plastic handle fire extinguishers and Kidde push-button Pindicator fire extinguishers, which have been sold throughout the United States since January 1, 1973.The recall of the Kidde fire extinguishers with plastic handles includes 134 models that were manufactured from January 1973 to August 15, 2017, and includes models that were previously recalled in March 2009 and February 2015.The plastic handle fire extinguishers were sold in red, white, and silver and are either ABC- or BC-rated and have the model number printed on the fire extinguisher label. Units that were manufactured after 2007 have the date of manufacture in a 10-digit date code printed on the side of the cylinder, near the bottom. Digits five through nine represent the date and year of manufacture. Units manufactured prior to 2007 are not equipped with date codes.The recalled push-button Pindicator extinguishers brands includes eight different models that were manufactured between August 11, 1995 and September 22, 2017. These models have no-gauge push-button activated extinguishers that were sold in red or white cylinders with a red or black nozzle. The Pindicator models were sold primarily for kitchen and personal watercraft applications.For a full list of the recalled models, manufacturing dates and model numbers, please visit the officialย CPSC recall notice.The products were sold at Menards, Montgomery Ward, Sears, The Home Depot, Walmart and various other department, home and hardware store nationwide as well as online through Amazon.com, ShopKidde.com and other online retailers for between $12 and $50, and for about $200 for the XL 5MR models. The extinguishers came as standard equipment with the purchase of some commercial trucks, recreational vehicles, personal watercrafts and boats.The recalled extinguishers were manufactured in the United States and Mexico. They were imported and distributed for sale through Walter Kidde Portable Equipment Company Inc., of Mebane, North Carolina.According to the CPSC, an estimated 37.8 million units were distributed for sale throughout the United States and another 2.7 million were sold in Canada.The CPSC recommends that consumers with the recalled fire extinguishers immediately contact Kidde to request a free replacement and to receive instructions on how to return recalled units. Affected consumers can contact Kidde by calling at 855-271-0773, or by visiting www.kidde.com and clicking on “Product Safety Recall.” 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: Burn, Fire, Fire Extinguisher Recall, KiddeMore Lawsuit Stories Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis July 21, 2026 Taco Bell Cyclospora Lawsuit Claims Contaminated Lettuce Caused Illnesses July 21, 2026 Roblox Predator Lawsuit Claims Adult Lured Minor Into Sending Explicit Pics on Instagram July 21, 2026 0 Comments EmailThis 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 Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (Posted: yesterday)A Dupixent cancer lawsuit claims the manufacturers failed to adequately test and label the eczema treatment, resulting in a CTCL cancer diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026)Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026) Fourth Uber Driver Sex Assault Lawsuit Bellwether Trial Set for Oct. 2026 (Posted: 2 days ago)A federal judge has scheduled the fourth bellwether trial involving claims that Uber failed to protect passengers from being sexually assaulted by its drivers for early October.MORE ABOUT: UBER SEXUAL ASSAULT LAWSUITUber Faces Investor Lawsuit Over Failure To Stop Driver Sexual Assaults (07/13/2026)Uber Sexual Assault Lawyers To Meet With MDL Judge Next Week, in Advance of Upcoming Trial (06/26/2026)Lyft Rideshare Assault Lawsuit Alleges Company Attempts To Silence Attack Victims (06/15/2026) Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (Posted: 5 days ago)Plaintiffs and defendants have submitted a joint schedule for a final pretrial conference before the second Bard PowerPort lawsuit bellwether trial over claims the port catheter is defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITNew Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)Jury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)
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