The Latest Breaking News from the Food and Drug Administration

The Food and Drug Administration found dead and live rodents, and their feces and urine. More than 1,200 rodents were exterminated after fumigation at the warehouse, which serves more than 400 stores.

The Food and Drug Administration has warned consumers against using "smart" devices that are marketed to measure blood sugar without piercing the skin.

Health officials reported 10 cases of E. coli infection, adding that the number of people sick is likely "much higher." Those cases were from California, Colorado, Texas and Utah.

People who are immunocompromised continue to worry about COVID. A raft of products promise protection. Is there any evidence they can protect from infection or lessen severity of disease?

UK-based company Haleon recalls eight batches of cough syrup over risk to immunocompromised individuals

The Checks and Balances Letter delivers news and information from Ballotpedia’s Administrative State Project, including pivotal actions at the federal and state levels related to the separation of powers, due process, and the rule of law.

While as little as one injection of penicillin G benzathine can cure syphilis, the shortage prompted U.S. health officials to recommend giving some patients another antibiotic that requires of weeks of twice-daily pills.

An excerpt from a long report and recommendation released Wednesday by Magistrate Judge Ona Wang (S.D.N.Y.) in Cassava Sciences, Inc. v. Bredt; for more details, read the whole opinion: At various dates in 2021, the Neuroscientist Defendants filed a Citizen Petition and sent publicly available letters to the Food and…

The Food and Drug Administration's authorization of Florida's plan to import prescription medicines from Canada is a first. But the state still has hurdles to clear before imports could begin.

Despite what appears to be a major medical breakthrough on treatments for Sanfilippo, the Food and Drug Administration has refused to funnel the medicine through a faster approval process.

In early December, the Food and Drug Administration approved a gene-editing treatment for sickle cell disease, the first for any illness. One patient helped pave the way.