News

FDA issues most serious risk warning for cheese recall
A recall of cheese curds over potential contamination with Listeria monocytogenes has received the highest risk warning from ...
Medical groups urge Kennedy, FDA to reexamine broad approval of abortion drugs
Pro-life medical groups are urging Health and Human Services Secretary Robert Kennedy Jr. to reexamine the FDA’s broad ...
Courthouse News Service2h
Judge revokes FDA injunction allowing abortion pill access
The ruling reverses the judge’s own decision from two years ago that allowed Washington state and 17 other states to continue ...
US FDA approves KalVista's oral swelling disorder drug, shares rise
KalVista Pharmaceuticals said on Monday the U.S. Food and Drug Administration has approved its drug, the first on-demand oral ...
FDA Layoffs Could Compromise Safety of Medications Made at Foreign Factories, Inspectors Say
Beyond staff cuts, the departures of some longtime investigators in recent months have left less experienced people tasked ...
Nationwide Gummies Recall Update as FDA Issues Highest Risk Warning
Vita Warehouse Corp. recalled more than 40,000 bottles of Vitamin B12 supplements for possible undeclared presence of peanut.
STAT1d
Inside the staff exodus and tanking morale that threaten Makary’s FDA
WASHINGTON — The steady erosion of experienced staff at the Food and Drug Administration is slowly compromising the agency’s ...
Healio9h
FDA approves SIR-Spheres for unresectable hepatocellular carcinoma
The FDA approved Y-90 resin microspheres for the treatment of unresectable hepatocellular carcinoma, according to a press ...
RFK Jr.'s FDA officials overrode career staff to limit COVID shots
The FDA's Dr. Vinay Prasad said that he disagreed with the agency's career vaccine reviewers about COVID shot approvals.
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Fed-up and demoralized, FDA staff are leaving.
This is the web edition of D.C. Diagnosis, STAT's twice-weekly newsletter about the politics and policy of health and ...
Healio11h
FDA approves expanded indication of pulsed field ablation systems for persistent AF
Boston Scientific announced the FDA approval of expanded labeling for its pulsed field ablation system which now includes ...
Insider Monkey5h
Syndax’s Revuforj Granted FDA Priority Review for Relapsed/Refractory Mutant NPM1 AML
On June 24, Syndax announced that the US FDA granted Priority Review for its supplemental New Drug Application (sNDA) for ...