The FDA has recalled some raw cat food — here’s what’s safe to give your pet instead
This weekend, the FDA announced that two types of Savage Pet raw cat food are being recalled for potential contamination with ...
Food Recalls, Updates March 17: Chowder and Pet Food Products Removed
Seafood chowder and a pet food product have been recalled over risk of serious illness and bird flu contamination, ...
FDA allows companies to decide what food additives are safe. That may be changing.
The Food and Drug Administration lets companies self-report whether a chemical they add to food is safe. That may be changing ...
RFK Jr. wants to eliminate FDA’s controversial food additive program. Here’s why that matters
It’s time to revamp the FDA’s “generally recognized as safe,” or GRAS, program that allows companies to add untested ...
The FDA Cracking Down on Compounded Weight Loss Drugs – Here’s What It Means for Telehealth Companies and Consumers
After years of weight loss drug shortages, the FDA is saying there’s now an adequate supply for most medications and they ...
FDA voices ‘concerns’ with unapproved GLP-1 drugs used for weight loss
FDA is aware that some patients and health care professionals may look to unapproved versions of GLP-1 – glucagon-like peptide-1 receptor agonists – drugs, including semaglutide and tirzepatide, as an ...
How the FDA lets chemicals pour into America's food supply
Chemicals such as titanium dioxide and potassium bromate, whose safety has been debated, are allowed in foods in the United ...
Grocery Dive5h
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 ...
Scientific American3d
Scientist’s Study Led FDA to Ban Red No. 3 Food Dye. Yet He Says It Is Safe
Joseph Borzelleca published a study on the food coloring Red No. 3. The FDA cited his work when banning the additive in ...
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FDA Determines REMS No Longer Necessary for Tryvio
The Tryvio REMS program was established due to the risk of birth defects associated with the ERA drug class. Prior to dispensing Tryvio, patients of reproductive potential were required to report a ...