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.
FDA Unveils New Plan To Improve Response to Food Poisoning OutbreaksThe plan comes as food poisoning outbreaks have doubled in recent years, according to the FDA’s findings. December 15, 2021 Russell Maas Add Your CommentsRegulatory officials have released a new food poisoning outbreak plan, which will use modern technology to quickly pinpoint potential sources of contamination and expedite the release of investigation findings, as part of an effort to reduce the risk of additional illnesses.The U.S. Food and Drug Administration (FDA) released the Foodborne Outbreak Response Improvement Plan last week, which includes strategies to enhance the speed, effectiveness and communication of foodborne outbreak investigations to both the industry, but also consumers.Food poisoning impacts an estimated 48 million Americans annually, resulting in an average of nearly 130,000 hospitalizations and 3,000 fatalities, according to the U.S. Centers for Disease Control and Prevention (CDC). These outbreaks sicken on average one out of every six Americans and cost about 15.6 billion each year.The new food poisoning outbreak response plan was released under the FDAโs Food Safety Modernization Act (FSMA) and New Era of Smarter Food Safety initiative, focusing on four specific priority areas in which the FDA, CDC, U.S. Department of Agricultureโs Food Safety Inspection Service (FSIS), and state health officials can strengthen outbreak responses.The plan first outlines how the FDA will collaborate with participating agencies to engage in tech-enabled product traceback investigations to more quickly identify the source of contaminated foods. Often with foodborne illness outbreaks, it can take weeks or even months to identify the source of an outbreak, which allows harmful products to remain on store shelves and in consumerโs homes, resulting in additional injuries and deaths.The plan also seeks to streamline the data sharing process among the investigating agencies as well as consumers to provide a more accurate and transparent process that may include public warnings to avoid certain types food items that could be related to the outbreak.Additional efforts outlined in the plan include centralizing data among agencies to better identify reoccurring, emerging and persistent strains of pathogens, as well as building on performance measures for evaluating the timelines and effectiveness of outbreak investigation activities.The new response plan was introduced following an independent review led by the University of Minnesota, School of Public Health. The independent report titled An Independent Review of FDAโs Foodborne Outbreak Response Processes, was performed to give an objective assessment of the FDAโs structural and functional capacity to support, participate in, or lead multistate foodborne illness outbreak investigation activities.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 COMPENSATIONOver the last several years, some have raised questions over whether the U.S. food supply has become less safe, or if the increased number of E. coli outbreaks, salmonella outbreaks and listeria outbreaks are due to the agencies becoming better at detecting threats to the U.S. food supply.The FDAโs Coordinated Outbreak Response and Evaluation Network indicates the amount of potential human food safety outbreak incidents per year doubled in 2017 and 2018 when compared to the 2015 and 2016 fiscal years.The FDA has proposed several new technologies and tracing methodologies in an effort to enhance traceability, respond more rapidly to outbreaks, address new business models, reduce contamination of food, and foster the development of stronger food safety cultures.Last week the FDA issued the Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption Relating to Agricultural Water last week, which would require comprehensive testing and bacteria mitigation strategies for water sources used for crops if approved and finalized.The proposed rule changes would require an annual assessment of farmsโ pre-harvest agricultural water to identify potential hazards. They would then manage their agricultural water quality based on the results of that assessment, implementing corrective or mitigation measures to reduce the risk of contamination.Foodborne illness outbreaks linked to produce are common in the U.S since they are often not adequately treated after being harvested to remove pathogens, and it is also one food group that is commonly eaten raw by consumers, rather than being cooked to kill bacteria. 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: Food PoisoningMore Food Poisoning Lawsuit Stories E. Coli Food Poisoning Lawsuit Filed Over Recalled Organic Carrots November 21, 2024 Charcuterie Meat Salmonella Outbreak May Be Linked to Under Processing: FSIS February 14, 2024 FDA Finalizes New Rule to Make Food Poisoning Outbreaks More Traceable November 16, 2022 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)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: 3 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: 4 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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