Recently, a jury ordered Bayer AG’s Monsanto unit to pay more than $2.2 billion, $250 million in compensatory damages and $2 billion in punitive damages, to John McKivison, a 49-year-old former Roundup user who argued that the herbicide he used at home and at work caused his non-Hodgkin’s lymphoma, a…
Illinois Injury and Mass Tort Lawyer Blog
Expert Weighs in on Stanley Tumbler’s Lead Scare
As you likely already know, Stanley tumblers are trendy water bottles. They are so popular that the Valentine’s day limited edition version of the tumbler triggered physical confrontations and campouts at Target. They are often used as a fashion accessory and the company’s use of influencers on social media has…
Ozempic Lawsuits Have Been Centralized in Pennsylvania Court
Recently, the United States Judicial Panel on Multidistrict Litigation centralized the Ozempic lawsuits, at least 55 of them, in Pennsylvania federal court. These lawsuits allege that defendants Novo Nordisk and Eli Lilly failed to warn people of severe side effects linked to the diabetes and weight loss drugs Ozempic and…
Amazon, Target and Walmart Will Stop Selling Water Beads
Three of the United States’s largest retailers, Amazon, Target, and Walmart, have announced they will no longer sell water beads, which are often marketed for children with development disorders. The beads are made of polymers, and in water, they can expand about 150-1500 times their original size. Public pressure has…
FDA Questions Whether Applesauce Pouches Were Contaminated Intentionally
As we’ve previously related on this blog, the United States Food and Drug Administration has recalled three applesauce products. These products include WanaBana apple cinnamon fruit puree pouches, Schunks cinnamon applesauce pouches, and Weis cinnamon applesauce pouches. The recall stems from the FDA’s investigation of dozens of acute lead poisonings…
The FDA Warns Consumers to Check Philips DreamStation 2 CPAP Machines for Signs of Overheating
The Philips DreamStation 2 CPAP machine, used both at home and in medical settings, is prescribed to provide positive airway pressure for treatment of obstructive sleep apnea. Recently, the United States Food and Drug Administration (FDA) has warned patients and health care providers to diligently attend to whether their Philips…
Toy Magnets Linked to 7 Deaths and 2,400 Hospitalizations
Recently, federal safety regulators asked consumers to stop buying and using magnetic toy ball sets for their children’s use. These magnetic balls have now been associated with hundreds of serious injuries as well as 7 fatalities, 5 of them within the U.S. When swallowed, these toys magnets may attract to…
Autopilot Software Recalled in 2 Million Tesla Vehicles
Tesla makes almost 50% of the electric passenger cars sold in the United States. Recently, however, Tesla recalled more than 2 million of its cars. Previously, to no avail, federal regulators had pressed Tesla to update its Autopilot system, which can accelerate, steer, and brake by itself, and to make…
Baxter Issues Urgent Medical Device Correction for Novum IQ Syringe Infusion Pump
Recently, Baxter International, Inc. announced that its Novum IQ syringe infusion has the potential to provide an incomplete infusion. It issued an Urgent Medical Device Correction for the product. The company is developing a software upgrade to fix the problem. There have been no serious injuries reported so far. However,…
FDA Issues Warning of Rare but Serious Drug Reaction to the Antiseizure Medicines
The United States Food and Drug Administration (FDA) recently warned consumers that certain antiseizure medications can cause a rare but serious response called Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS). When not diagnosed and treated rapidly, these can prove fatal. The affected seizure medications are levetiracetam (Keppra, Keppra XR,…