News

Urgent product recall issued after glass fragments found in everyday essential
A food staple – bread – has been recalled after glass fragments were found on the top surface of some loaves. Upper Crust ...
The Daily Signal5mOpinion
Shocking Data Shows Far Higher Risks of Mifepristone Than FDA Claimed
A shocking report on mifepristone has finally shown a light on how the FDA is harming, and even killing, thousands of women.
FOX 2 Detroit25m
FDA plans to remove petroleum-based food dyes; dietitian explains the impact
Petroleum-based synthetic dyes are typically used to add color to highly processed foods like cookies, candy and cereal.
FDA chief says they're looking at whether to approve COVID shots for next winter
The head of the Food and Drug Administration said Tuesday that the agency is now looking at whether it will still approve COVID-19 vaccines for next winter, citing a lack of data on booster shots.
California settles suit over toxic seafood. Here's what to know to eat fish safely
The California Attorney General settled with three food companies found to have sold seafood with elevated levels of lead and cadmium.
Telehealth patients get access to more weight-loss drugs
Click in for more news from The Hill{beacon} Health Care Health Care   The Big Story Novo Nordisk partners with telehealth ...
FDA announces ban for compounded weight loss drugs
Recently, the FDA announced the removal of certain compounded GLP1 ingredients from its drug shortage list. These ingredients ...
FDA Commissioner Makary says agency will focus on "gold-standard science and common sense"
Dr. Marty Makary has been outspoken about vaccine mandates and other public health measures, so how does the Food and Drug ...
Santa Cruz Sentinel2h
Martinelli’s voluntarily recalls more than 170,000 apple juice bottles due to potential toxin contamination
More than 170,000 bottles of apple juice produced by Watsonville-based S. Martinelli & Co. have been taken off the shelves ...
The Indiana Gazette2h
FDA Approves Zevaskyn for Rare, Genetic Skin Disorder
The U.S. Food and Drug Administration has approved Zevaskyn (prademagene zamikeracel) for patients with the rare, genetic skin disorder recessive dystrophic epidermolysis bullosa.
FDA Chief Says He Won’t Reorganize Agency After Mass Layoffs (1)
The FDA doesn’t plan to execute a reorganization of the agency but will consolidate offices that handle travel, technology, ...