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.
Queseria Bendita Cheese and Sour Cream Recall Issued After Listeria Death January 20, 2015 Russell Maas Add Your CommentsFollowing at least two reports of illness and one death due to listeria poisoning, a number of soft cheese and sour cream products sold primarily at Hispanic grocery stores in Washington and Oregon are being recalled.ย A Queseria Bendita recall was announced by the FDA on January 16, following reports linking the cheese and sour cream products to an outbreak of listeria food poisoning.The recall includes all lots of Panela, Queso Fresco, Requeson, and Cotija fresh soft cheese and sour cream products with โBest Byโ dates up to April 16, 2015. The recalled cheese and sour cream products may be identified by matching the brand name with the correlating UPC codes and Best By dates.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 products include the following; Panela brand with UPC code 610074 99341 4 and best by date code 041615, Queso Fresco brand with UPC code 0 94922 10602 5 and best by date code 041615, Queso Fresco brand name with no UPC code and best by date code 041615, Requeson brand name with UPC code 0 94922 10603 2 and best by date code 041615. Sour Cream/ Crema Agria brand name with UPC code 0 94922 10608 7 with no best by code, and Cotija Cheese brand name with no other identifiable codes or dates.The products were manufactured by Queseria Bendita LLC, of Yakima, Washington and packaged in 1lb. or 3lb. plastic wrappers or plastic tubs and contain a shelf life of up to 90 days. All products were distributed to Hispanic grocery stores in Washington and Oregon and also the companyโs on-site store in Yakima, Washington.Listeria infections may result in symptoms such as nauseam 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, listerosis can pose a risk of miscarriages, still births, premature delivery or life-threatening infection of the newborn.Radar Farms Fresh Smoothie RecallA second listeria-related recall was announced the same day by federal health officials, involving Rader Farms Fresh Smoothie Blends. The smoothies were manufactured by Inventure Foods, Inc. of Pheonix, Arizona and may also be contaminated with listeria monocytogens, although no illnesses have been recorded in connection with the four recalled brands of fusions and smoothie blends.The recall includes Fresh Start Smoothie Blend sold at Costco and Costco Canada in 48 oz. containers with UPC code 884038851489, Fresh Start Sunrise Refresh Fusion products sold at Walmart in 35 oz. containers with UPC code 884038851540, and Fresh Start Daily Power Fusion smoothie blends sold at Walmart in 35 oz. containers with UPC code 884038851533. The products were distributed to major retailers such as Walmart and Costco in Alaska, Arizona, California, Colorado, Idaho, Montana, New Mexico, Oregon, Utah, Washington, Texas, and in Alberta, British Columbia, Manitoba, and Saskatchewan of Canada.The FDA is alerting consumers that they may not experience symptoms immediately following consumption and if believed to have consumed any recalled products to consult with their healthcare provider immediately. Sometimes reports of illness may take up to two months past the time of consumption due to the time it takes for patients to experience symptoms and get a diagnosis.Customers and store owners with recalled Queseria Bendita soft cheese and sour cream products should remove them from store shelves or from the home and destroy the products and contact the company at 509-961-8949 for further questions.Consumers and retailers with recalled Queseria Bendita are encouraged to destroy the products. Consumers with questions can call the company at (509) 961-8949. Customers with recalled Rader Farms smoothie blends are encouraged to return them to the place of purchase for a full refund. Those with questions can contact Inventure Foods Customer Service at (866) 890-1004 or sen an email to info@inventurefoods.com or visit the company’s website at RaderFarms.com/FreshStartRecall. 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: Cheese Recall, Food Poisoning, Listeria, Oregon, WashingtonMore 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 InstagramThis 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: 2 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: 3 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: 4 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)
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