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.
Atkins, Kashi, Numerous Other Companies Impacted by Expanded Sunflower Seed Recall June 7, 2016 Irvin Jackson Add Your CommentsA nationwide sunflower seed recall has been widely expanded, impacting dozens more manufacturers and products that may be contaminated with listeria monocytogens, a bacteria that may cause serious and sometimes fatal infection.ย SunOpta announced a sunflower seed kernel recall expansion on June 1, which affects additional products sold across the nation to retailers and wholesalers. To date, no incidents of listeria food poisoning have been reported since the original recall in May this year.In conjunction with the U.S. Food and Drug Administration (FDA), SunOpta announced the original sunflower seed recall on May 4, after routine testing confirmed the presence of listeria within sunflower seed kernels processed at the Crookston, Minnesota facility. SunOpta relayed to retailers that certain sunflower products could have been exposed to listeria contamination during processing prompting several recalls at the retailer level.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 COMPENSATIONAlthough neither SunOpta nor the FDA has announced exactly how many pounds of sunflower kernels are included in the massive recall, well over 100 products have been recalled from major retailers across the nation including Trader Joeโs, Wal-Mart, Kroger, Giant Eagle, Brown & Haley, Market District, Meijerโs, JayโC, Dillons, Bakers, Gerbes, King Soopers, City Market, Fryโs, Ralphs, Food 4 Less, Smithโs and various others.The original recall included all sunflower kernel products originating from SunOptaโs Minnesota facility between the dates of February 1, 2016 and February 19, 2016. SunOptaโs recent recall expansion now covers all sunflower kernel products produced at the facility between May 31, 2015 and January 31, 2016 for potential listeria monocytogen contamination.Since the recall expansion, at least a dozen or more recalls have been initiated by retailers due to the potential for their products to have been processed with listeria contaminated sunflower kernels from SunOpta.On June 1, Publix Super Markets issued a multi-state recall for various nut, seed, and raisin mixes after being notified by their supplier Flagstone Foods that the sunflower products originated from SunOptaโs Minnesota facility. The products were sold in the produce sections of Publix supermarkets across six southern states.Several popular product recalls were announced on June 3, by Kashi Company forย various types of sunflower butter spreads and chewy granola bars, Atkins Nutritionals Inc. who announced recalls for various flavored granola bars and yogurt products, Quaker Oats Company who announced recalls of two popular flavors of granola bars, and Cliff Bar Company who announced three popular flavors of energy bars.Listeriosis is a foodborne illness that can cause serious health consequences and death, especially for children, the elderly and those with weakened immune systems. The infection is considered by the FDA as one of the more dangerous foodborne illnesses and frequently results in hospitalizations and carries a 25% fatality rate.Symptoms of listeria infections may include nausea, muscle ache, diarrhea, fever, and fatigue. In severe cases for the elderly and young children, the bacteria could spread through the bloodstream to the nervous system resulting in sometimes fatal infections. For pregnant women, listeriosis can pose a risk of miscarriages, still births, premature delivery or life-threatening infection of the newborn.Affected products were likely shipped to nearly every state in the U.S. and Canada since May 2015. Customers are being urged to search the open recalls for products potentially contaminated with SunOpta sunflower kernels. Retailers and wholesalers are being asked to check their inventories and shelves to confirm that none of the recalled products are present or available for purchase by consumers.The FDA is also asking customers to check their inventories at home and to take any remaining products back to their store of purchase for a refund or simply discard them. Customers may contact SunOpta for further information at 1-888-886-4428 or email the company at emailcontactus@sunopta.com. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Listeria, Listeria Food Poisoning, Sunflower Seed RecallMore Lawsuit Stories Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides October 20, 2026 Chemo Port Fracture Lawsuit Alleges SmartPort Problems Led to Removal Surgery October 20, 2026 Tylenol Autism and ADHD Lawsuits Advance as Appeals Court Rejects Rehearing October 20, 2026 0 Comments PhoneThis 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 Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: today)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026) Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: yesterday)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026) Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: 4 days ago)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)
Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: today)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)
Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: yesterday)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)
Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: 4 days ago)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)