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.
Tainted Cucumbers Recalled Due to Salmonella Food Poisoning Risk January 4, 2016 Russell Maas Add Your CommentsAmid continuing efforts to reduce the risk of food poisoning outbreaks associated with produce sold throughout the U.S., a recall has been issued for almost 175 bulk-packed containers of cucumbers that tested positive for salmonella, which may cause a serious and potentially fatal infection for those with weakened immune systems.ย A Thomas Produce Cucumber recall was announced by the FDA on December 31, after the agency yielded a positive result for salmonella during routine testing. To date, no cases of salmonella food poisoningย have been linked to the recalled cucumbers.The recall includes cucumbers farmed and processed by Thomas Produce Company of Boca Raton, Florida, which were sold in cardboard bushel boxes marked with lot numbers 1554311JDNK, 1554311HDNK, or 15143115DNK, and cardboard bins marked with lot codes 15NKJD-1554311-D, 15NKHD-1554311-D, or 15NK5D-1514311-D.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 recalled cucumbers were sold to distributors in Florida and Georgia between December 15, 2015 and December 16, 2015, but may have been sold throughout the region. Thomas Produce Company and the FDA have notified all potential distributors to remove any remaining products from store shelves and to thoroughly check any remaining inventory.For healthy individuals, salmonella symptoms typically include diarrhea, nausea, vomiting, and abdominal pain lasting between 4 and 7 days. The illness can become worse due to the delay in treatment because the infection can only be diagnosed by testing stool samples and is usually treated with antibiotics.Among individuals with a weakened immune system, such as the elderly, children or pregnant women, the illness can pose a much greater risk and may lead to death or still birth if left untreated. In rare circumstances, the infection can even spread throughout the blood stream and cause arterial infections, endocarditis and arthritisCustomers should stop consuming the recalled cucumbers immediately and either dispose of them or return them to their place of purchase. The FDA recommends during these broad โbulk-boxedโ recalls that consumers always err on the side of caution if you cannot identify if a cucumber is part of a recall, and throw it away. For further information, customers may contact Thomas Produce Company at 1-561-482-1111.Produce Food Poisoning OutbreaksOver the last several years, the United States has steadily been the victim of multi-state outbreaks from foodborne bacteria infecting produce and vegetables both imported and home-grown. The Centers for Disease Control and Prevention (CDC) estimates 48 million people are sickened each year from food poisoning, 130,000 are hospitalized from the infections, and another 3,000 result in fatalities.In September, the CDC announced an outbreak of Salmonella Poona linked to cucumbers grown in Mexico and imported by Andrew & Williamson Fresh Produce. The CDCโs last update in October reported that 838 consumers across 36 states had been diagnosed with the infection and caused 157 hospitalizations and four deaths.In September 2014, the FDA identified a Salmonella Newport outbreak through their national molecular subtyping network for foodborne disease, PulseNet. The outbreak investigation identified similar strains of infection found in 275 individuals from 29 states that linked back to cucumber farmers in Marylandโs Eastern Shore in the Delmarva region. Several other major cucumber outbreaks have occurred over the last few years, including the Salmonella Saintpaul outbreak that sickened 73 people from 18 states due to tainted cucumbers imported from Culiacan, Mexico.The FDA announced a new series of food safety rules in November 2015, for produce farms and food importers to adopt science-based contamination prevention methods, food sampling and testing requirements, and to allow for third party auditors to certify facilities are meeting FDA food safety requirements.Incorporated into the Food Safety Modernization Act (FSMA), the new rules are designed to help remove and mitigate any or all possible threats of dangerous bacteria contaminating imported produce. 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: Cucumber Recall, Salmonella, Salmonella Food PoisoningMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit 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) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)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)
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Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit 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)
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