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.
Mad Cow Disease Fears Lead To Beef Recall June 13, 2014 Russell Maas Add Your CommentsA recall of more than 4,000 pounds of fresh ground beef products has been initiated, after government food inspections agencies idicated that the beef may be infected with bovine spongiform encephalopathy (BSE), which is more commonly known as Mad Cow Disease.ย The Rain Crow Ranch Ribeye beef recall was announced by the U.S. Food Safety and Inspection Service (FSIS) on June 11, following a review of the manufacturerโs slaughter logs, which indicated specific materials were not removed from the beef products that may allow them to be infected with BSE. To date, no illnesses or deaths have been reported.During the processing of beef products, โspecified risk materialsโ are removed from cattle during the slaughter process to prevent contamination. Specifically, the dorsal root ganglia that branches from the nervous system located in the vertebral column are considered high risk materials.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 COMPENSATIONAccording to FSIS regulations, these kinds of tissues and other are to be removed from cattle 30 months of age and older due to the fact they are more likely to contain the infective agent Bovine Spongiform Encephalopathy, or mad cow disease.The infectious agent that causes mad cow disease is an abnormal version of a protein normally found on cell surfaces, called a prion. Typical use of heat to cook meats to kill infections does not work with prions and they remain in the food. Symptoms of mad cow can take up to 13 months to surface and can consist of depression, loss of coordination, and in later stages can cause dementia, brain abnormalities and even death.The FSIS noticed the potential for these specified beef products to be infected when reviewing the companyโs slaughter logs. The FSISโs investigation indicates the company employees were recording information and determining the age of various cattle incorrectly, potentially allowing cattle containing the aged dorsal root ganglia to pass inspection without removal.The recalled beef products were manufactured by Fruitland American Meat Company of Jackson, Missouri on various dates ranging from September 2013 to April 2014.Recalled products include 40-lb. cases of โRain Crow Ranch Ribeyeโ steaks containing roughly two 20-lb. cryovac packages of bone-in bearing the establishment number โEST. 2316โ inside the USDA mark of inspection. The beef products were marked with the production dates 9/5/13, 9/10/13, 9/11/13, 9/26/13, 10/2/13, 10/3/2013, 11/8/13, 11/22/13, 12/17/13, 12/26/13, 12/27/13,1/16/14, 1/17/14, 1/23/14, 1/31/14, 2/13/14, 2/14/14, 2/21/14, 2/28/14, 3/8/14, 3/20/14, 4/4/14 or 4/25/14 printed on the box. The quartered beef carcasses were stamped with the USDA mark of inspection and have establishment number EST.2316.The beef products were known to have been distributed to a restaurant in New York and a Whole Foods distribution center in Connecticut. Beef carcasses were known to have been distributed to a plant in Missouri and a restaurant in Kansas City, Missouri. All recalled beef products would have been cut and packaged separately with no identifying marks on the consumer packaging.The recall has been classified as a Class II recall meaning there is a remote probability of adverse health consequences from consumption of the beef products.The FSIS is advising consumers to be cautious of adverse health effects after consuming ribeye beef products from the distributed states and to consult with their healthcare provider if necessary. Customers may also contact Fruitland American Meatโs sales manager James Fortner at 573-243-3107 with further questions regarding the recall. 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: Beef Recall, Bovine Spongiform Encephalopathy, Brain Infection, Food Poisoning Image Credit: |More Lawsuit Stories Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 May 29, 2026 Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed May 29, 2026 Top Fitness Lawsuit Claims Home Gym Machine Failed, Crushing Womanโs Legs May 29, 2026 0 Comments CommentsThis 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 Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (Posted: today)The second Bard PowerPort bellwether trial is now scheduled to begin in August after the plaintiff in a claim originally planned for trial next month died, and her family stopped pursuing litigation.MORE ABOUT: BARD POWERPORT LAWSUITJury Returns Defense Verdict in First Bard PowerPort Injury Lawsuit (05/11/2026)Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (04/16/2026)Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026) Dupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (Posted: yesterday)A Delaware woman has filed a Dupixent lawsuit, claiming manufacturers promoted the eczema drug as a breakthrough treatment while failing to warn that it may trigger or worsen CTCL, a rare form of non-Hodgkinโs lymphoma.MORE ABOUT: DUPIXENT LAWSUITLink 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)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026) Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 2 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
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Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: 2 days ago)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)