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.
Widespread Vegetable Recall Hits Safeway, Whole Foods, Meijers And Others Over Listeria Risk October 24, 2017 Russell Maas Add Your CommentsA major vegetable supplier is recalling various products that were distributed throughout the United States and Canada, due to a potential risk that they may be contaminated with bacteria that causes listeria food poisoning.ย The Mann Packaging multi-state vegetable recall was announced by the FDA on October 19, after routine testing by the Canadian Food Inspection Agency identified listeria monocytogens. To date, the FDA has not received any reported illnesses in relation to the recall.Included in the recall are various minimally processed vegetables and mixed vegetable products that were packaged and distributed by Mann Packing of Salinas, California to grocery and retailer chains across the United States and Canada.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 FDA indicates the products were sold under various brand labels, including Signature Farms, HEB, and Walmart, but were all packaged by the Mann Packing Company. The recalled items are marked with โBest If Used Byโ dates from October 11, 2017 through October 20, 2017. For a full list of the recalled items and UPC codes, please visit the FDAโs product recall list.The recall affects a wide variety of vegetable products, such as cauliflower, broccoli, Brussels sprouts, and mied vegetable medleys. To date, the FDA is aware of the potentially contaminated products being distributed to at least eight states in the U.S. and various retailers and distributers in Canada.Since Mann Packaging announced its recall, several major food chain retailers have released subsequent recalls including Wal-Mart, Trader Joeโs, Whole Foods Market, Signature Farms, Meijer, Albertsons, Safeway, and Vons and Pak Nโ Save and various other in at least eight states to prevent a multi-state outbreak.Listeria is a food borne illness that can cause serious health consequences and can be fatal, especially for children, the elderly and those with weakened immune systems. The infection poses a significant threat to pregnant women, who may be at an increased risk for miscarriages or still-births.The symptoms of listeria infection typically include nausea, muscle ache, diarrhea, fever, and fatigue. In severe case, listeria may become more life threatening when the infection moves through the bloodstream into the nervous system resulting in sometimes fatal infections.Mann Packaging indicates that it is cooperating with local and federal officials in both the U.S. and Canada to have any and all potentially contaminated products removed from store shelves. Customers who are unsure if a certain product in included in the recall should refrain from consumption until verified.Customers who believe they are in possession of the recalled vegetables should stop consuming the products immediately and contact Mann Packaging at their 24-hour consumer line at 888-470-2681 or visit them at veggiesmadeeasy.com/products. 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: Listeria, Listeria Food Poisoning, Trader Joe's, Vegetable Recall, Walmart, Whole FoodsMore Lawsuit Stories Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit May 19, 2026 Cartiva Toe Implant Erosion Resulted in Persistent Pain, Lawsuit Alleges May 19, 2026 Amazon Ladder Collapse Lawsuit Claims Defective Device Caused Permanent Injuries May 19, 2026 0 Comments FacebookThis 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 Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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) Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit 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) SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026)
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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)
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SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026)