Hosted on MSN1h
FDA recalls in 2025: The 8 products pulled from shelves by US food safety after death
The Food and Drug Administration have seen a number of food items pulled from the shelves since the start of 2025, with the ...
STAT1d
Leaving FDA, Califf is unapologetic — and warns of staff departures
In an interview, outgoing FDA commissioner Robert Califf was wary of the Trump administration but unapologetic about ...
cidrap.umn3h
GAO to FDA: Inspect more domestic, foreign food facilities to ensure safe food supply
On average, the FDA conducted 8,353 routine domestic and 917 foreign food-facility inspections per year from 2018 through ...
STAT7d
Save the Food and Drug Administration by breaking it up
Snake oil, it turns out, motivated the founding of the FDA. The term “snake oil” arose out of a controversy from the late ...
Medscape1h
No-Implant Shunt Wins FDA Breakthrough Status for Heart Failure
The new approach is designed to create a connection between the left and right atrial chambers of the heart in a single ...
The FDA Set Guidelines for 'Acceptable' Levels of Lead in Baby Food for the First Time — but Some Experts Say It's Not Enough
On Monday, the U.S. Food and Drug Administration (FDA) announced that, for the first time, it is setting guidelines for an ...
ConsumerAffairs4h
Watchdog report finds FDA lags in food inspection duties
The U.S. food supply is generally considered safe, but tens of millions of people get sick from foodborne illnesses each year ...
FDA Sets New Levels for Toxic Lead in Baby Food
The FDA's new standards for toxic lead target processed baby foods such as jarred fruits, vegetables, yogurts and dry cereals ...
JD Supra3h
FDA Updates Final Guidance on Cosmetic Facility Registration and Product Listing: Wiley
The Food and Drug Administration (FDA) recently issued a Notice announcing the availability of an updated final guidance for the industry ...
JD Supra4h
FDA issues Guidance on Interim Animal Food Ingredient Consultation (AFIC) Process
Center for Veterinary Medicine (CVM) issued its final guidance on the interim Animal Food Ingredient Consultation (AFIC) process, which FDA positions as a stopgap measure to temporarily replace FDA’s ...
Cure Today55m
FDA Grants BTD to the ADC GSK’227 in Relapsed/Refractory Osteosarcoma
The FDA has granted BTD to GSK’22, a B7-H3-targeted antibody-drug conjugate, for the treatment of adult patients with ...
Exelixis Notified by FDA That Cabozantinib Application Won't Be Discussed at Meeting
Exelixis said it was notified by the Food and Drug Administration that its treatment for advanced pancreatic neuroendocrine tumors and advanced extra-pancreatic will not be discussed at a meeting.