Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks
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.
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
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.
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.
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.
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 Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks October 21, 2026 SpaceOAR Lawsuit Alleges Prostate Cancer Treatment Caused Rectal Fistula, Required Colostomy October 21, 2026 Study Links HeartMate 3 LVAD to Neurological Risks October 21, 2026 0 Comments X/TwitterThis 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 Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (Posted: today)A woman’s Boston Scientific Spectra WaveWriter SCS lawsuit claims improper hermetic seals lead to short circuits, failures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026) Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: yesterday)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026) Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: 2 days ago)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)
Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks October 21, 2026
SpaceOAR Lawsuit Alleges Prostate Cancer Treatment Caused Rectal Fistula, Required Colostomy October 21, 2026
Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (Posted: today)A woman’s Boston Scientific Spectra WaveWriter SCS lawsuit claims improper hermetic seals lead to short circuits, failures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)
Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: yesterday)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)
Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: 2 days ago)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)