FDA investigating illnesses linked to raw cheddar cheese from California farm

A raw cheese producer has declined to issue a recall of two of its products after the Food and Drug Administration linked the ...

FDA Announces E. Coli Outbreak Linked to Cheddar Cheese—Here’s What to Know

While there is no formal recall currently in place, check your refrigerator. If you have the cheddar cheese on hand, the FDA ...

FDA authorizes F10 wound spray to combat New World screwworm

Texas Agriculture Commissioner Sid Miller praised the U.S. Food and Drug Administration’s decision to authorize emergency use ...

Multivitamin recall update for 25 states as FDA sets risk level

It was voluntarily initiated after a U.S. Food and Drug Administration inspection found the product was deficient.

FDA approves new use of synthetic vitamin B9 — but not for autism symptoms

The FDA announced a new approved use for the drug leucovorin, which Trump has touted as a treatment for autism. But the ...

FDA doesn’t approve leucovorin for autism. What can it be used for?

The FDA narrowed leucovorin's use to a rare disorder, a major shift after Trump and RFK Jr. promoted it for autism.

Cheese recall update as FDA sets most serious risk level

The FDA issued its most serious risk classification—Class I—on March 11, according to the official enforcement notices.

Cream Cheese Recalled by FDA for 'Serious Adverse Health Consequences or Death,' Marking Agency's Highest Warning Level

Multiple flavors of Made Fresh Salads' cream cheese are affected by the recall ...
Becker's Hospital Review

FDA advisers recommend fall flu shot changes

FDA advisers recommend fall flu shot changes to include the new subclade K H3N2 variant for the 2026-27 season, improving vaccine relevance.

No Broad Autism Approval for Leucovorin, Despite FDA Commissioner’s Prior Suggestions

The Food and Drug Administration on March 10 changed the approval for a version of the prescription drug leucovorin to include people with a very rare genetic condition. FDA Commissioner Dr. Marty ...

FDA sends warning letter to Novo Nordisk over failure to report deaths, adverse side effects of GLP-1s

The U.S. Food and Drug Administration (FDA) has issued a warning to Novo Nordisk over its alleged failure to report adverse side effects, including death, in patients who took its GLP-1 medications, ...
CBS News

Inside the FDA's vaccine uproar

Dr. Céline Gounder, an internist, epidemiologist and infectious disease specialist, is a CBS News medical contributor as well as senior fellow and editor-at-large for public health at KFF Health News.