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.
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 Lawsuit Alleges Roblox Sexual Predator Convinced 8-Year-Old Girl To Send Him Explicit Videos May 14, 2026 Ozempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk May 14, 2026 Gourmia Pressure Cooker Lawsuit Alleges Lid Interlock Failure Caused Life-Altering Burn Injuries May 14, 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 Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: yesterday)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026) Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: 2 days ago)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026) Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 3 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)
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