Mercedes Recalling S-Class Sedans Over Steering Problem
Mercedes-Benz is recalling 6,200 S-Class sedans, coupes, and convertibles from model years 2018-2019 over a software problem in the automated steering system which could result in a crash and/or great bodily injury, the U.S. National Highway Transportation Administration (NHTSA) announced...
Mississippi Woman Files Blood Clot Filter Lawsuit
A lawsuit has been filed by a woman who has an IVC Filter permanently embedded in her body because it is too dangerous to remove.
Sausage Sold in Ohio Recalled for Lack of Inspection
Jugo’s, Inc. of Parma, Ohio, has issued an urgent recall for its Balkan Style Sausage after it was found that the products failed to undergo a state inspection.
FDA Warns Against Using “Young Blood” for Anti-Aging Therapy
The FDA says there is no proof that transfusions of "young blood" actually work for anti-aging or illness treatments, and they are worried that consumers are being duped into paying up to $12,000 per infusion as they seek the Fountain...
Dukkah (Egyptian Dip) Recalled for Glass Contamination
A Massachusetts company is recalling cans of Jansai Valley Brand Dukkah from retailers across the U.S. over concerns they may contain tiny pieces of glass, which could ruin your day if you’re not careful.
Academy Sports + Outdoors Recalls Turkey Fryers for Fire Hazard
Academy Sports + Outdoors is recalling about 3000 turkey fryers due to a fire hazard.
Honda Recalls Trucks for Fire Hazard After Car Washes
Honda has recalled 106,683 of the model-year 2017, 2018, and 2019 Ridgeline trucks because they can catch on fire after being washed.
Nature’s Path Recalls Gluten-Free Cereal for Undeclared Gluten
Nature's Path Foods is recalling more than 416,000 boxes of its kids' gluten-free cereal in the U.S. and Canada over concerns it may contain an "undeclared gluten," the U.S. Food & Drug Administration (FDA) warned on Friday.
Baby Gripe Water Recalled Over Undissolved Ingredient
Bottles of an herbal supplement for infants are being recalled across the U.S. due to the presence of an undissolved ingredient, the U.S. Food & Drug Administration (FDA) announced on Friday.
FDA Issues Class 1 Recall for Over 150K Medtronic Pacemakers
The FDA has announced a Class I recall for approximately 156,957 pacemakers manufactured by Medtronic due to a software error that could lead to a lack of pacing.