FDA upgrades Oregon, Washington recall for Lay's Classic Potato Chips to highest level
The FDA upgraded a recall for Lay's Classic Potato Chips to the highest risk level for packages distributed in Oregon and ...
Recall for broccoli sold at Walmart in 20 states upgraded to highest risk level: FDA
The Food and Drug Administration has upgraded its classification of a broccoli recall initially reported in late December, ...
Courthouse News Service1d
Oregon defends drug pricing transparency law before Ninth Circuit
The state refuted the argument that its prescription drug pricing transparency law compels pharmaceutical companies to disclose trade secrets.
FDA classifies Lay’s recall as Class 1 due to undeclared milk allergen
Last month, a recall was issued for Lay’s Classic Potato Chips sold in Oregon and Washington due to the potential presence of ...
Chocolate Recall Updated to Highest Risk Level, FDA Warns Consumption Could Cause Death
The FDA has updated the December recall of some of Cal Yee Farms' products to the highest risk level classification for three ...
FDA elevates Lay's potato chip recall in Oregon, Washington to highest risk level
Class I, according to the FDA, means exposure to or consumption of the product could cause "serious adverse health ...
Statesman Journal6d
FDA upgrades Oregon, Washington recall for Lay's Classic Potato Chips to highest level
According to an FDA alert, packages delivered to Oregon and Washington as early as Nov. 3, 2024 “may contain undeclared milk” and “those with an allergy or severe sensitivity to milk run ...
Oregon bill sparks debate over drug testing for unemployment benefits in certain cases
Senate Bill 748 would permit the Employment Department to conduct drug testing on individuals filing for unemployment if they ...
FDA approves first new type of pain medication in 25 years
A new pain relief drug, suzetrigine, is a prescription pill that’s taken every 12 hours after a larger starter dose. It will ...
FDA elevates Lay's potato chip recall to highest risk level
Class I, according to the FDA, means exposure to or consumption of the product could cause "serious adverse health ...