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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
E. Coli Food Poisoning Risk Results in Marketside Butcher and Thomas Farms Ground Beef Recall June 15, 2020 Russell Maas Add Your CommentsMore than 40,000 pounds of raw ground beef products sold by Walmart and other retailers are being recalled, due to a risk of E. coli food poisoning.The ground beef recall was announced by the U.S. Food Safety and Inspection Service (FSIS) on June 13, after routine testing at a Lakeside Refrigerated Services production facility discovered the presence of E. coli O157:H7 in certain raw ground beef products. No incidents of E. coli food poisoning have been linked to the meat, but it may pose a serious risk for consumers nationwide.The recall involves approximately 42,922 pounds of mostly grass-fed ground beef products manufactured by Lakeside Refrigerated Services of Swedesboro, New Jersey, which were produced on June 1, 2020 and distributed throughout the United States under the Marketside Butcher and Thomas Farms brands, with a United States Department of Agriculture (USDA) mark of inspection number โEST. 46841โ.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 affects 1-lb. vacuum packages containing โMARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEFโ, 1-lb. vacuum packages containing four ยผ lb. pieces of โMARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEF PATTIESโ, 3-lb. vacuum packages containing three 1 lb. pieces of โMARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEF 93% LEAN / 7% FATโ, 1-lb. tray packages containing four ยผ lb. pieces of โTHOMAS FARMS GRASS-FED GROUND BEEF PATTIES 85% LEAN / 15% FATโ, 4-lb. tray packages containing 10 ยผ lb. pieces of โTHOMAS FARMS GRASS-FED GROUND BEEF PATTIES 80% LEAN / 20% FATโ, 1-lb. vacuum packages containing four ยผ lb. pieces of โTHOMAS FARMS GRASS-FED GROUND BEEF PATTIES 85% LEAN / 15% FATโ, and 1-lb. vacuum packages containing โVALUE PACK FRESH GROUND BEEF 76% LEAN / 24% FATโ.Customers are being warned the products may still be in refrigerators or freezers at this time. Any remaining products should be either discarded or returned to their place of purchase.FSIS officials have classified the recall as Class I, indicating it is the most serious of its kind and that the consumption or use of the product has a high probability of resulting in serious adverse health consequences or death.E. coli is a foodborne bacteria that causes mild to severe diarrhea and abdominal cramps, bloody stools, and sometimes minor fevers lasting between five and 10 days. For individuals like young children, the sick and the elderly, the consequences may be more severe due to weakened immune systems, potentially resulting in the infection causing a serious condition known as Hemolytic Uremic Syndrome (HUS), which may lead to kidney failure or even death.Customers with recalled products are being asked to either throw them away or return them to their place of purchase. For additional questions or concerns regarding the recall customers may contact the Lakeside Processing Center Call Center at (856) 832-3881. 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: E. Coli, E. Coli Food Poisoning, Food Poisoning, Ground Beef Recall, Hemolytic Uremic SyndromeMore Lawsuit Stories Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial October 6, 2026 Lawsuit Alleges FreeStyle Libre 3 Plus, iLet Insulin Pump Device Failures Caused Death October 6, 2026 Uber Sexual Assault Settlement Reached Before Bellwether Trial Begins October 6, 2026 0 Comments InstagramThis 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 Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial (Posted: today)A federal judge has selected the third claim to serve as a Covidien hernia mesh bellwether trial, which will begin in March.MORE ABOUT: HERNIA MESH LAWSUITJudge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (09/11/2026)Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026) Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: yesterday)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026) Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 4 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)
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