FDA staff return to crowded offices, broken equipment and missing chairs
Thousands of Food and Drug Administration employees are returning to the office to find overflowing parking lots, cramped ...
FOX 9 Minneapolis-St. Paul1h
Food products including macaroni and cheese bites recalled for 'undeclared eggs'
Small Bites Macaroni & Cheese packages were recalled on Friday by C.H. Guenther & Son LLC of San Antonio, Texas, due to the ...
Grocery Dive11h
RFK Jr wants to close a ‘loophole’ in food additive regulation
The Health and Human Services Secretary directed the FDA to consider eliminating a pathway that allowed companies to ...
Popular macaroni and cheese recall sparks warning nationwide
Two food products from two different companies have been recalled over the past 24 hours due to the presence of “undeclared ...
‘Our food is literally killing us’: FL lawmakers propose warning labels for certain foods
Concerns around ultra-processed foods and synthetic dyes have state lawmakers pushing legislation to ban chemical additives ...
Food Recalls, Updates March 14: H-E-B Dip, Chocolate Nut's Risk Level Set
A recalled spinach artichoke dip is a Class II risk, and updates have been issued for the recall of chocolate nut and wafer ...
FDA cracks down on popular gay party drug ‘poppers’
While poppers have previously been incorrectly linked to AIDS in the LGBTQ+ community — an unfounded stance Robert F. Kennedy ...
F.D.A. Issues Warning About Galaxy Gas and Other Nitrous Products
The agency is advising people to avoid misusing or inhaling the products that are marketed as whipped cream chargers but have ...
RFK Jr. Wants to Close a Controversial FDA Loophole in Food Additive Regulation
The FDA’s GRAS rule lets companies decide if food additives are safe—without agency oversight. RFK Jr. now aims to close this ...
The BMJ5d
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study
Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...