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.
Cottonelle Wipes Class Action Lawsuit Filed Over Bacterial Infection, Illness Risks November 23, 2020 Russell Maas Add Your CommentsFollowing a massive recall issued last month for Cottonelle flushable wipes, a class action lawsuit alleges that consumers have developed serious bacterial infections and illnesses that resulted from contaminated products distributed this year.The complaint (PDF) was filed by Dawn Rothfeld in the U.S. District Court for the Eastern District of New York on November 19, indicating that Kimberly-Clark Corporation negligently manufactured and sold the wipes without following proper sanitary protocols, which caused products to become contaminated with Pluralibacter gergovaie, which is an opportunistic pathogen capable of causing potentially harmful infections in humans.Kimberly-Clark issued a recall of Cottonelle Flushable Wipes and Cottonelle GentlePlus Flushable Wipes last month, after it was discovered that products sold exclusively at Costco stores may be contaminated with the microorganism bacteria.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 lawsuit seeks class action status to pursue damages for all individuals from New York who purchased the products between February 7, 2020 and September 14, 2020, indicating that many of the recalled wipes had dark-brown spots on the surface and mildew-like odors emanating from the packeting, which should have been detected by the manufacturer as a clear indicator of bacterial contamination.“But Kimberly-Clark’s investigation was neither prompt nor careful,” according to the complaint. “Only after a rash of customer complaints regarding skin irritation, infection and other complications became overwhelming (and thus a reckoning, inevitable) did Kimberly-Clark conduct the investigation and product testing required to discover the bacterial contamination.”Pluralibacter gergovaie poses a particularly serious risk among those with pre-existing medical conditions, those who have recently undergone surgery, and other categories of consumers. Prior outbreaks of the pathogen have been difficult to treat, as some strains are antibiotic resistant.The lead plaintiff in the complaint, Dawn Rothfeld, indicates that she purchased the now-recalled Cottonelle wipes in February, and began using them frequently after bowel movements. As a result of exposure to the bacteria, Rothfeld indicates that she suffered suffer various injuries, including urinary tract infections, painful and urgent bladder pressure, painful urination, and increased frequency of urination due to infection of Pluralibacter gergovaie.Rothfeld was placed on antibiotic therapy by her doctor and was required to undergo radiological studies, including ultrasounds of the abdomen and bladder. As a result of the infection, Rothfeld continues to suffer from pain, weakness, fatigue, stomach discomfort, nausea, vomiting, and difficulty walking and severe emotional trauma.According to allegations raised in the Cottonelle Wipes class action lawsuit, Kimberly-Clarke neglected to take steps that would have protected consumers, and continued to sell the product for months without warning the public, resulting in widespread injuries.“The Recall has affected thousands of consumers who purchased the Wipes at retail locations, causing damages that include loss of value, personal injury, and violation of consumer protection and deceptive practices statues, as detailed herein,” Rothfeld indicates in the complaint. “Further, Kimberly-Clark has left thousands of consumers holding packages of Cottonelle Flushable Wipes that are unsuitable for their intended use and, thus, entirely worthless.”Rothfeld claims that an “alarming number” of consumers have reported problems from Cottonelle wipes during the eight months before the recall, including various symptoms consistent with P. gergoviae infections, ranging from general discomfort to severe infections. Thousands of women have also reported urinary tract infections after using the wipes, as well as other injuries that may have gone undiagnosed due to the rare strain of bacteria involved.According to the recall notice, consumers who purchased recalled Cottonelle Flushable Wipes or Cottonelle GentlePlus Flushable Wipes should stop using the product immediately, and contact Kimberly-Clarkโs Consumer Service team at 1-800-414-0165 for further instructions 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: Bacterial Contamination, Cottonelle, Infection Image Credit: |More Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 2 Comments fredda December 27, 2021 Suffered from bladder infections. Tina November 24, 2020 Suffered a series of bladder & GI infections having to take antibiotics repeatedly. Meading to weak immune system. Kimberly Clark offered me “peanuts.” Do I have a case! 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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 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 Womanโs 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 AngioDynamicsโ 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 Womanโs 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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