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.
Listeria Food Poisoning Outbreak Prevention Measures Updated by USDANumerous listeria food poisoning outbreaks in recent months have caused federal safety officials to reanalyze their inspection processes. December 19, 2024 Michael Adams Add Your CommentsA series of recent listeria food poisoning outbreaks has prompted federal food inspectors to re-evaluate their review processes and implement several improvements aimed at protecting Americans from severe illnesses in the coming year.Following a number of high-profile listeria outbreaks earlier this year, the U.S. Department of Agricultureโs (USDA) Food Safety and Inspection Service (FSIS) issued a press release on December 17, announcing that the agency will be taking stronger measures to protect the American public from listeria bacteria, starting as early as January 2025.Listeria monocytogenes is a foodborne bacterium that causes listeriosis, an illness characterized by fever, muscle aches, nausea, vomiting and diarrhea. While symptoms are often mild in healthy individuals, children, the elderly and those with weakened immune systems face a higher risk of severe complications, including hospitalization and death.Pregnant women and their unborn children are particularly vulnerable to listeriosis. The infection can lead to devastating outcomes, such as premature delivery, miscarriage, or stillbirth, even if the mother experiences only mild symptoms.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 FSIS has announced plans to enhance its review processes in response to concerns over listeria contamination. While the evaluation remains ongoing, the agency has identified three key areas for improvement, with changes set to take effect within 30 days:Enhancement of science-based approaches to stop the spread of foodborne pathogens, which will include increased testing of ready-to-eat products, environments and food contact surfacesImprovement to tools and training for inspectors, by updating and standardizing inspector instructions, as well as conducting Food Safety Inspections and Assessments through in-person visits and follow-upsEvolution of oversight for facilities that the agency regulates, including regular inspections of listeria-related risk factors at ready-to-eat manufacturing plants, and revising alert triggers for further establishment reviewsโAs a science-based regulatory agency, USDAโs Food Safety and Inspection Service is constantly looking at ways we can and should evolve our processes to protect the public, maintain confidence in Americaโs food supply, and prevent foodborne illness,โ USDA Under Secretary for Food Safety, Dr. Emilio Esteban, said.Boarโs Head Deli Meat Listeria Outbreak and OthersThe FSIS announcement comes on the heels of a major Boarโs Head deli meat listeria outbreak that occurred earlier this year.Boarโs Head initiated a recall of deli meat products that had been tainted with listeria bacteria on July 26. The injuries caused by this outbreak resulted in a number of Boarโs Head listeria outbreak lawsuits, including several wrongful death lawsuits filed on behalf of individuals who died, as well as a class action lawsuit on behalf of all consumers exposed to the tainted deli meats.In addition to the Boarโs Head listeria outbreak, there have been numerous other listeria-related outbreaks and recalls in recent months. These include a BrucePac recall of nearly 10 million pounds of ready-to-eat meat, as well as a frozen waffle recall over listeria risks, traced to TreeHouse Farms products that were sold at Walmart, Target and other major grocery chains. Written by: Michael AdamsSenior Editor & JournalistMichael Adams is a senior editor and legal journalist at AboutLawsuits.com with over 20 years of experience covering financial, legal, and consumer protection issues. He previously held editorial leadership roles at Forbes Advisor and contributes original reporting on class actions, cybersecurity litigation, and emerging lawsuits impacting consumers. Tags: Boar's Head Recall, Brucepac Recall, FSIS, Listeria, Listeria Food Poisoning, Listeria Monocytogenes, Listeriosis, TreeHouse Foods Recall, USDA Image Credit: Shutterstock: Tada ImagesMore Lawsuit Stories Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 September 11, 2026 DraftKings Lawsuit Indicates ‘Event Contracts’ Are Nothing More Than Sports Bets September 11, 2026 Social Media Wrongful Death Lawsuit Links Major Platforms to Child Suicides September 11, 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 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: today)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: yesterday)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 2 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: today)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: yesterday)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 2 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)