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.
Recalled Hy-Vee Spring Pasta Salads Linked To Nearly 80 Illnesses: CDC August 2, 2018 Russell Maas Add Your CommentsFederal health officials warn that nearly 80 individuals have been sickened as part of a multi-state salmonella outbreak, which has been linked to certain Spring Pasta salads, calling on consumers to check their refrigerators and to discard the products immediately.ย The U.S. Centers for Disease Control and Prevention (CDC) released a multi-state food poisoning outbreak warning on August 1, alerting consumers that certain Hy-Vee Spring Pasta Salads have been recalled after trace back investigations determined the products may contain Salmonella, a serious and sometimes fatal foodborne illness.The CDCโs update indicates that at least 79 individuals across nine states have fallen ill with similar strains of Salmonella, resulting in eighteen hospitalizations. To date, no deaths have been reported in relation to the recall.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 pasta salad recall was first issued by the FDA on July 17, after Hy-Vee, Inc. received at least 20 reports of consumers being diagnosed with salmonella food poisoning.The recall includes Hy-Vee Spring Pasta Salads that were packaged in both one pound and three pound containers. The potentially contaminated products were produced from June 1 through July 13 and were distributed to all 244 Hy-Vee grocery stores in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.According to the recall notice, the expiration date for the impacted products range from June 22, 2018 through August 3, 2018. Expiration information can be found on the side of the containers.Consumption of food contaminated with Salmonella can cause salmonellosis and seriously sicken the affected person. Salmonellosis is one of the most common food borne illnesses. Symptoms of the illness include, diarrhea, abdominal cramps, and fever typically within 12 to 72 hours after eating the tainted product and may last for up to 4 to 7 days. While most patients recover without needing medical treatment, in some more serious cases, patientโs diarrhea may be so severe they need hospitalization and IV fluids.The FDA recommends that anyone who handled the potentially recalled products thoroughly wash their hands, containers, utensils or surfaces that could have come in contact with the products to prevent further spread of contamination.Hy-Vee announced they have removed all known contaminated products from store shelves and are advising consumers to check their refrigerators and discard any recalled pasta salads or return it to the store of purchase for a full refund. Customers with additional questions or concerns may contact Hy-Vee Customer Care at 1-800-772-4098. 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 Poisoning, Hy-Vee, Pasta Salad Recall, SalmonellaMore Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 0 Comments CompanyThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: today)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: yesterday)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 2 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026
NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: today)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026)
Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: yesterday)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 2 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)