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.
Cargill Ground Beef Recall Issued Amid Salmonella Outbreak July 24, 2012 Ricky Allen Add Your CommentsNearly 30,000 pounds of Cargill ground beef are being recalled due to concerns that it may be responsible for a salmonella food poisoning outbreak that has sickened at least 33 people in seven states.ย The Cargill ground beef recall was announced by the U.S. Department of Agricultureโs Food Safety and Inspection Service (FSIS) on July 22, due to concerns that meat produced and distributed by Cargill Meat Solutions may be contaminated with Salmonella Enteritidis.The action was taken as the result of a multi-state salmonella infection outbreak, which has resulted in illnesses in Massachusetts, Maine, New Hampshire, New York, Rhode Island, Virginia and Vermont.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 COMPENSATIONWorking in conjunction with the Centers for Disease Control and Prevention (CDC), Vermont Department of Health, New York State Department of Health, and New York State Department of Agriculture & Markets, FSIS was able to link illnesses in five case-patients to the ground beef distributed by CargillThe recall affects 29,339 pounds of meat labeled “Grnd Beef Fine 85/15,” sold in cases containing three 14 pound chub packages. The meat has an establishment number of “EST. 9400” inside the USDA mark of inspection. These products were produced on May 25, 2012, and were shipped to distribution centers in Connecticut, Maine and New York for further distribution. The meat was likely repackaged and sold under other labels and retail brand names.Even though the use-by date has passed, the concern is that people may still have the products frozen in their freezers at home.Salmonella is a type of bacteria that attacks the gastrointestinal tract, causing mild to severe food poisoning. For most healthy adults, symptoms of food poisoning from salmonella typically resolve after a few days or weeks. However, young children, the elderly, and individuals with compromised immune systems have an increased risk of suffering severe food poisoning after ingesting the bacteria. If not properly treated, some cases of salmonella food poisoning can lead to hospitalization, dehydration or death.Salmonella serotype Enteritidis (SE) is one of the most common serotypes of Salmonella bacteria reported worldwide. The strain of Salmonella Enteritidis associated with the ground beef recall is not antibiotic resistant.FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160ยฐ F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature.This is the second year Cargill has been the subject of a major meat recalls. Last year, a massive ground turkey recall was issued for 36 million pounds of meat produced by the company. That meat was believed to have been contaminated with Salmonella Heidelberg, which was suspected to have caused at least 79 illnesses across the U.S., including at least one death. Cargill faced a number of food poisoning lawsuits as a result of that ground turkey recall.Consumers with questions about the latest Cargill recall can call the company’s consumer information line at (888) 812-1646. Tags: Cargill, Ground Beef Recall, Maine, Massachusetts, New Hampshire, New York, Rhode Island, Salmonella, Salmonella Food Poisoning, Vermont, Virginia Image Credit: |More Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 1 Comments Isangela October 1, 2012 Depend on your own instincts. The FDA is still sleeipng with the Industry. You can Count on That! Always,to little to late in doing their jobs. If the laws are unenforcable why have a useless Agencies such as these. Wasting tax dollars to parade the wants and needs of Corporate demands at the expense of the Consumer.To prove the extent of the Bed Buddy program.We have seen these agencies persuaded Not to Label Genetically Modified Foods .So Consumers Have no Choice in the products they Eat. Government has betrayed the trust of the people.So what makes them any better than Sadamn Hussan? 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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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 4 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 5 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 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)
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