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.
Kidde Plastic Fire Extinguisher Recall Issued After Reports of Failures February 13, 2015 Russell Maas Add Your CommentsAn estimated 4.6 million Kiddie plastic fire extinguishers have been recalled, after safety officials received nearly a dozen reports of the extinguishers failing to discharge, increasing the risk of serious injury or property damage in a fire.ย The U.S. Consumer Product Safety Commission (CPSC) announced a Kiddie disposable fire extinguisher recall on February 12, following reports that the extinguishers failed to discharge.At least 11 consumers have reported the plastic fire extinguishers failed to work when needed. However, no injuries have been reported in connection with the extinguishers.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 has determined that the problem is linked to a faulty valve component. The extinguishers may not fully discharge when the lever is repeatedly pressed and released during a fire, the commission warns.The recall includes 31 models of Kiddie disposable fire extinguishers with Zytel black plastic valves sold in either red, white, or silver canisters. The extinguishers are rated ABC or BC for multi-purpose use. Ratings can be located on the right-hand side of the nameplate. Recalled extinguishers were manufactured between July 23, 2013 and October 15, 2014 and possess a 10-digit date code that is stamped near the bottom on the cylinder. The last five digits of the date code indicate the day and year of manufacture in DDDYY format. Date codes for recalled unites manufactured in 2013 are XXXX201413 X through XXXX36513 X and those produced in 2014 are XXXX 00114 X through XXXX28814 X.Affected fire extinguishers will have one of the following model numbers affixed on a nameplate on the front; 10BC, 1A 10BC, 1A 10BCW, 2A10BC, 5BC, 5BCW, FA10G, FA110, FA5B, FC10, FC110, FC5, FH/RESSP, FX10, FX10BC, FX10K, FX210, FX210R, FX210W, FX340GW, FX340SC, FX5II, KFH Twin, M110 Twin, M5 Twin, Mariner 10, Mariner 110, Mariner 5, Mariner 5 G, RESSP, and XL 5MR. About 4.6 million units were sold in the United States, and about 175,000 were sold in Canada.The recalled models were manufactured in Mexico and imported by Walter Kiddie Portable Equipment Company Inc., of Mebane, North Carolina. They were sold at Home Depots, Menards, Walmart, and other department, home and hardware stores nationwide and online from August 2013 through November 2014 for between $18 and $65, and about $200 for the XL 5MR model.The CPSC recommends that customers check their fire extinguishers to see if they are affected by the recall. Customers with recalled extinguishers should contact Kiddie at 855-283-7991 or visit them online at www.kiddie.com and navigate to the Safety Notice for information on how to obtain a free replacement fire extinguisher. 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: Fire, Fire Extinguisher Recall, KiddieMore Lawsuit Stories Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims June 16, 2026 Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges June 16, 2026 EnfaCare Preterm Infant NEC Lawsuit Alleges Formula Caused Life-Threatening Diagnosis June 16, 2026 0 Comments CommentsThis 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 Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: yesterday)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026) Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (Posted: 2 days ago)A tentative Depo-Provera lawsuit settlement has been announced, vacating the start of the first bellwether trial while details are finalized.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026)Depo-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) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 5 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)
Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: yesterday)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)
Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (Posted: 2 days ago)A tentative Depo-Provera lawsuit settlement has been announced, vacating the start of the first bellwether trial while details are finalized.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026)Depo-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)
Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 5 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)