The U.S. Food and Drug Administration has delayed reviews of two drugs chosen for the Trump administration's new fast-track ...

Designation underscores the potential of this chemically induced, off-the-shelf cell therapy to address a high unmet need in ...

Sarah Todd returned to reporting in January 2025 after being assignment editor at STAT since October 2022. You can reach Sarah on Signal at sarahlizchar.47. The infant botulism outbreak that sickened ...

U.S. Food and Drug Administration (FDA), After Reviewing Historical Use and Modern Safety Evidence, Officially Confirms Kava is a Food Under Federal Law This federal confirmation, issued through ...

The U.S. Food and Drug Administration and the European Medicines Agency jointly issued principles for safe and responsible ...

The Food and Drug Administration has warned four major retailers that they failed to meet statutory requirements to make sure their stores removed ByHeart infant formula after it was recalled. The ...

In a Nov. 17 warning letter the Food and Drug Administration outlined problems at Bedner Growers Inc. of Boynton Beach, FL, which is the company that sold cucumbers traced to outbreaks of Salmonella ...

Regulators at the U.S. Food and Drug Administration on Monday gave the green light to a pill version of the blockbuster weight-loss drug Wegovy, the first daily oral medication to treat obesity. The ...

Over 83,000 bags of raw shrimp from Indonesia are being recalled, the FDA said. The FDA has announced a recall of frozen raw shrimp due to potential exposure to the radioactive isotope cesium-137. The ...

The FDA granted fast track status to VectorY’s VTx-002, an antibody gene therapy targeting TDP-43 protein aggregates in ALS.

Stacey Leasca is an award-winning journalist with nearly two decades of newsroom experience. She is also the co-founder of Be a Travel Writer, an online course for the next generation of travel ...