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.
Zilmax Feed Additive Sales Halted Amid Cattle Problems August 19, 2013 Martha Garcia Add Your CommentsFollowing recent concerns about the effects of Zilmax feed additive on cattle, Merck has halted sales of the product pending further investigation.In a statement issued Frida, Merck & Co. announced that sales of the widely popular animal feed additive Zilmax will be suspended.The decision comes after an earlier statement on August 8, where the drug maker announced that it will launch an internal study into the risk of cattle problems from Zilmax, after reports surfaced that suggested the additive may cause lameness in some animals.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 COMPENSATIONZilmax is a popular beta-agonist, a class of drugs used to add weight to cattle, pigs and turkey before slaughter. It is given to the animal for only 20 days, but Merck reports the product increases carcass weight by 24 to 33 pounds, while improving tenderness and flavor in the beef.Tyson Foods, the nationโs largest meat processor, recently announced that it will no longer accept beef from cattle treated with Zilmax. The decision came after cattle that had been given Zilmax were observed having difficulty walking and moving. The company says the final decision was based on animal welfare; however many industry experts point to Zilmax as the cause.Amid the cattle problems, Zilmax sales will temporarily be halted in the United States and Canada, offering Merck time to conduct the study of the beef additive. Merck plans to establish study protocols, identify feeders and packers to participate in the study which will be overseen from the โfeed yard to the packing plant.โ The company also said it plans to create a third party team to validate the results of the study.The company continues to maintain that Zilmax is safe, citing 30 studies since 2007 which validate itโs safety. The FDA will work with Merck along with the U.S. Department of Agriculture to help determine the safety of the product.Livestock analysts were surprised by Merckโs decision, considering that the companyโs earlier announcement about the intention to further study the product did not include a plan to stop sales. Merckโs decision may have come as a result of the slew of recent bad press concerning Zilmax and itโs side effects on animals.Following Tysonโs announcement, JBS USA, a large U.S. Cattle processor, released a video of cattle exhibiting the same signs of lameness that Tyson reported. The video shows cattle having difficulty walking after being fed beta-agonist additives.Analysts say the Zilmax cutback could result in a reduced supply of beef starting in the fall; however beef producers and livestock analysts say they do not expect significant changes. They anticipate companies currently using Zilmax will switch to Optaflexx. Optaflexx is a less potent beta-agonist sold by Eli Lilly and Coโs Elanco animal health unit. It is less effective at adding weight to animals than Zilmax.Cargill, the third largest meat producer and major rival to Tyson Foods, said they will continue to buy cattle fed Optaflexx, calling Merckโs decision to halt Zilmax sales โprudent.โAnalysts predict the halt of Zilmax sales could result in a one percent drop in the production of beef in the U.S. Sales of Zilmax reached nearly $160 million last year alone. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. 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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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 3 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 4 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 5 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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