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.
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
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.
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.
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.
AngioDynamics Port Catheter 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.
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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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 Comments A 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. 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 manufacturer’s 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, “specified risk materials” 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… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION According 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 company’s slaughter logs. The FSIS’s 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 “Rain Crow Ranch Ribeye” steaks containing roughly two 20-lb. cryovac packages of bone-in bearing the establishment number “EST. 2316” 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 Meat’s sales manager James Fortner at 573-243-3107 with further questions regarding the recall. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell 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 nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Beef Recall, Bovine Spongiform Encephalopathy, Brain Infection, Food Poisoning Image Credit: | More Lawsuit Stories Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 January 27, 2026 Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant January 27, 2026 Study Questions Link Between Side Effects of Nexium, Prilosec and Stomach Cancer January 27, 2026 0 Comments URLThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: yesterday) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025) Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 2 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020) Proposed Depo-Provera Lawsuit Schedule Calls for First Trial in Dec. 2026 (Posted: 5 days ago) Lawyers involved in Depo-Provera litigation have agreed to hold the first bellwether trial over brain tumor injuries beginning on December 7, 2026. MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Indicates Depo-Provera Meningioma Diagnosis Followed Memory Loss, Dizziness Symptoms (01/20/2026)Depo-Provera Lawyers Intending To Remain in MDL Leadership Must Seek Reappointment: Judge (01/14/2026)Side Effects From Depo-Provera Shots Led to Brain Tumor, Multiple Surgeries: Lawsuit (01/06/2026)
Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 January 27, 2026
Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (Posted: yesterday) As Bard PowerPort litigation nears its first bellwether trials, the prospect of major jury verdicts over catheter fracture, migration and infection injuries is increasing speculation that settlement talks may intensify, following earlier claims that Becton Dickinson says were resolved in about 18 months before consolidation into a federal MDL. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide (12/05/2025)
Abbott Eterna Spinal Cord Stimulator Lawsuit Filed Over Lead Migration, Device Malfunction (Posted: 2 days ago) A spinal cord stimulator lawsuit claims an Abbott Eterna device failed after only two months due to lead migration. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lawsuit Claims Lead and Battery Problems Led to Multiple Revision Surgeries (10/22/2025)Medtronic Spinal Cord Stimulator Lawsuit Alleges Device Worsened Pain (04/30/2025)FDA Tells Doctors To Conduct Trial Stimulation Test Before Using Spinal Cord Stimulators (09/04/2020)
Proposed Depo-Provera Lawsuit Schedule Calls for First Trial in Dec. 2026 (Posted: 5 days ago) Lawyers involved in Depo-Provera litigation have agreed to hold the first bellwether trial over brain tumor injuries beginning on December 7, 2026. MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Indicates Depo-Provera Meningioma Diagnosis Followed Memory Loss, Dizziness Symptoms (01/20/2026)Depo-Provera Lawyers Intending To Remain in MDL Leadership Must Seek Reappointment: Judge (01/14/2026)Side Effects From Depo-Provera Shots Led to Brain Tumor, Multiple Surgeries: Lawsuit (01/06/2026)