The Food and Drug Administration has authorized Juul's original vaporizer and flavored cartridges to remain on the U.S.

Technology Technology The Big Story Stablecoin bill clears House in key crypto victory The House passed a bill setting up a ...

After a federal ban in 2022 kneecapped the popular vape company, the Food and Drug Administration, under the watch of MAHA ...

Within the first seven months of his second term, Trump has managed to add trillions to the deficit, eviscerate agencies like ...

The FDA has removed the REMS requirements for existing BCMA- and CD19-directed CAR-T therapies and reduced certain other post-infusion restrictions.

The FDA is shutting the door to imports of certain endoscope hardware manufactured by Olympus, saying that a production site in Japan has failed to meet quality requirements. | The FDA is shutting ...

In one of the first major tests of the new FDA leadership’s regulatory philosophy toward gene therapies for rare diseases, the agency is investigating two Duchenne muscular dystrophy patient ...

FDA requires updated warning about rare heart risk with COVID shots Myocarditis emerged as a complication after the first shots became widely available in 2021.

The FDA is amplifying a recall from Medtronic for its acid reflux testing system, after the company said it received 33 reports of serious injuries related to the device.

The FDA's Class I recall—reserved for fears of serious health issues or death—applies to about 3,200 cases of frozen shrimp distributed to Whole Foods stores.

The US Food and Drug Administration (FDA) has issued an early alert for three Medtronic pH-monitoring capsule devices. The notice follows two letters sent in June to customers by the devices ...

The U.S. Food and Drug Administration is now requiring two common COVID-19 vaccines to update their warning labels to include information on two rare heart side effects: myocarditis and pericarditis.