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.
Daily Harvest Class Action Lawsuit Filed Over Gastrointestinal IllnessesClass action lawsuit seeks damages for consumers nationwide who experienced gastrointestinal illnesses from Daily Harvest Crumbles July 1, 2022 Russell Maas Add Your CommentsFollowing hundreds of reports involving severe illnesses among individuals who ate frozen “French Lentil + Leek Crumbles” distributed by Daily Harvest, a class action lawsuit has been filed that seeks damages on behalf of consumers nationwide who experienced problems.A Daily Harvest recall was first announced last week, impacting nearly 30,000 packages of the prepared Crumbles distributed to individuals who subscribe to the popular meal delivery service. The action was taken after the manufacturer learned about more than 470 reports involving severe gastrointestinal illnesses, liver injuries and other injuries among consumers, often resulting in hospitalization. However, the exact source of the contamination remains unknown.In a complaint (PDF) filed in the United Stated District Court Southern District of New York on June 27, plaintiff Breeanne Peni states that she was one of the consumers who developed severe gastrointestinal illness after eating the recalled French Lentil + Leek Crumbles, which ultimately led to the need for surgical removal of her gallbladder.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 COMPENSATIONPeni indicates that after making an on-line purchase, the Daily Harvest food was delivered on May 24, 2022, and she consumed the French Lentil + Leek Crumbles on June 10, 2022. However, less than two days later, she was hospitalized after developing initial symptoms that included fever, nausea, extreme abdominal pain, chills and joint pain.The gastrointestinal illness from the Daily Harvest Crumbles caused Peni to require surgical removal of her gallbladder, and she had to remain hospitalized until June 17, 2022. She filed the complaint ten days later, seeking class action status on behalf of either all consumers nationwide, who received Daily Harvest French Lentil + Leek Crumbles distributed during April to June 2022.The lawsuit states the pain, suffering and bodily injury Peni experienced were a direct and proximate result of Daily Harvestโs negligence, in failing to exercise reasonable care in preparing and monitoring the safety and sanitary conditions of its French Lentil + Leek Crumbles. She also claims that Daily Harvest knew or should have known about the growing number of illnesses being reported by consumers, yet continued to market the new line of French Lentil + Leek Crumbles.Daily Harvest Lawsuit UpdateThe case is among the first of what are expected to be several hundred Daily Harvest lawsuits likely to be filed in the coming weeks and months.In aย Daily Harvest recall update issued Monday, the manufacturer stated that it is continuing to work with the FDA, the state Department of Agriculture and third party laboratories to inspect the facility where the food was manufactured, as well as food samples and multiple areas of the supply chain. However, Daily Harvest claimed that testing so far has failed to detect Listeria, E.Coli, Salmonella, Staphylococcus Aureus (Staph), B.Cereus, Clostridium species, mycotoxins, aflatoxins, or major allergens, including egg, soy, milk, and gluten.While the investigation continues, the FDA is instructing consumers to stop eating the recalled products and to discard them immediately to prevent further contamination and possible injury.There were only about 28,000 of the Daily Harvest packages distributed nationwide, but a shockingly high lumber of gastrointestinal illnesses and adverse reactions were reported. Since reported problems typically only account for between 1% and 10% of all injuries experienced by consumers, it is likely that the number of confirmed cases will continue to increase as individuals learn that the recalled Daily Harvest Crumbles may be responsible for their injury. 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: Class Action Lawsuit, Daily Harvest, Food Poisoning, Food Recall, Gastrointestinal, Liver DamageMore Lawsuit Stories Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications June 10, 2026 SteriCare Lawsuit Claims Compromised Sterile Saline Solution Caused Manโs Death June 10, 2026 Snapchat, Roblox Lawsuit Filed by Adult Sexually Exploited as a Child June 10, 2026 0 Comments CommentsThis 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 Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: yesterday)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026) Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: 2 days ago)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026) Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 3 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)
Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: yesterday)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: 2 days ago)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 3 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)