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.
Lean Cuisine Baked Chicken Meal Recall Over Contamination With Plastic Pieces December 21, 2020 Russell Maas Add Your CommentsFood safety officials indicate nearly 100,000 pounds of Lean Cuisine baked chicken meals may contain hard pieces of plastic, which could pose a choking or laceration hazard to consumers if swallowed.A Lean Cuisine baked chicken meal recall was announced by the U.S. Food Safety Inspection Service (FSIS) on December 19, after the manufacturer received several consumer complaints indicating large white pieces of plastic were found inside of certain Lean Cuisine white meat chicken with stuffing meals.Nestle Prepared Foods first discovered the problem on December 18, and an investigation determined one of the conveyor belts used during the production of the mashed potatoes had broken, potentially allowing varying sizes of hard white plastic to enter the products.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 recall includes approximately 92,206 pounds of Lean Cuisine Baked Chicken, white meat chicken with stuffing, red skin mashed potatoes and gravy meals sold in 8 5/8 ounce carton trays and marked with lot code 0246595911 and establishment number EST. P-9018. The impacted meals are marked with a Best Before date of October 2021.The products were manufactured by Nestle Prepared Foods of Springville, Utah and packaged on September 2, 2020. They were shipped to various retailers and distributors nationwide. A retailer distribution list is currently being compiled and will be posted on the FSIS website when available.Customers are being instructed to stop consuming the recalled products immediately and to check their freezers for any remaining inventory. All remaining recalled meals should be either discarded or returned to their place of purchase.The FSIS has categorized the recall as Class I, indicating there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death. To date, the agency has not become aware of any injuries related to the recall.Customers with questions about the recall can contact Nestlรฉ Prepared Foods, at (800) 993-8625. The U.S. Department of Agriculture also encourages consumers with food safety questions to call the toll-free USDA Meat and Poultry Hotline at 1-888-674-6854 or live chat viaย Ask USDA. 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: Food Recall, Lean Cuisine, PlasticMore Lawsuit Stories Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 June 25, 2026 U.S. Supreme Court Blocks Roundup Lawsuits Over Non-Hodgkin’s Lymphoma Warnings June 25, 2026 Pressure Cooker Explosion Lawsuit Alleges Recalled Crock-Pot Caused Severe Burn Injuries June 25, 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 Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (Posted: today)A federal judge has scheduled the first Dupixent lawsuit MDL initial case management conference for October 1, 2026.MORE ABOUT: DUPIXENT LAWSUITLawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (06/17/2026)Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026) Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: yesterday)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026) AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (Posted: 2 days ago)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)
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