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.
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
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.
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.
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.
Jenny-O Turkey Recall Issued Amid Food Poisoning Cases Reported Nationwide November 19, 2018 Russell Maas Add Your CommentsNearly 150,000 pounds of Jenny-O ground turkey products may be linked to a Salmonella outbreak, which has caused at least 164 food poisoning cases in 35 different states, with more than half of those sickened requiring hospitalization.Theย the U.S. Food Safety Inspection Service (FSIS) announced aย Jennie-O Turkey recallย on November 15, following after discovering that the raw meat contained the same strain of Salmonella involved in the outbreak.According to the FSIS, the ground turkey salmonella outbreak is ongoing, and other manufacturers and distributors of ground turkey products may be expected to issue recalls as the investigation continues.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 COMPENSATION“Ill people in this outbreak report buying many different brands of raw turkey products,” the U.S. Centers for Disease Control and Prevention (CDC) said in a similar statement. “A single, common supplier of raw turkey products or of live turkeys has not been identified that can account for all the illnesses in this outbreak.”The recall affects about 147,276 pounds of raw ground beef productsย sold in one pound packages distributed by Jenny-O, aย subsidiary of Hormel Foods Corporation. The recall came following a traceback investigation by the FSIS and the CDC, whichย determined Jennie-O ground turkey products contained matching strains of salmonella recovered from hospitalized patients.The action affects one pound packages of Jennie-O Ground Turkey 93% LEAN, Jennie-O TACO Seasoned Ground Turkey, Jennie-O Ground Turkey 85% LEAN, Jennie-O Italian Seasoned Ground Turkey and Ground Turkey 90% LEAN products that have โUse Byโ dates ranging from October 1, 2018 and October 2, 2018. The products are marked with establishment number P-190 inside the USDA mark of inspection and were shipped to a variety of retail locations nationwide.Hormel issued a statement late last week indicating the particular strain of salmonella is present in 29 different manufacturing plants from 19 different companies. The United States Department of Agriculture has not released the names of the other companies and manufacturing plants.Officials warn that the recalled ground turkey products should not be on stores shelves any longer, however, customers should check their freezers for any ground turkey products included in the recall and dispose of them immediately. According to FSIS officials, the outbreak has been ongoing since November 2017, with lab tests confirming salmonella cases in ground turkey, turkey patties, and live turkeys at farms and in pet food.With Thanksgiving approaching, FSIS officials are reminding consumers to always properly handle raw meat products to avoid spread of bacteria and cross contamination. Raw meat products should never be placed on counter surfaces where other food items are prepared, and utensils used to handle raw meat should be thoroughly washed after each use.Salmonella can cause symptoms such as severe cramps, diarrhea, chills, fever, headaches, bloody stools, nausea, and vomiting. Most symptoms last about four to seven days and can be treated at home.In some cases, those who get the infection experience serious complications, or symptoms that last weeks or months, or may require hospitalization. Young children, people older than 65, or those with weakened immune systems are especially at risk. 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: Ground Turkey, Ground Turkey Recall, Hormel, Salmonella, Salmonella Food PoisoningMore Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 0 Comments LinkedInThis 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 4 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 4 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)