SAN FRANCISCO, CALIFORNIA / ACCESS Newswire / January 2, 2026 / Jaguar Health, Inc. (NASDAQ:JAGX) ("Jaguar") today ...
The FDA designated the recall of certain Medtronic Bravo esophageal pH monitoring capsules as class I, the most serious type.
“FDA’s proposed rule, ‘Use of Formaldehyde and Formaldehyde-Releasing Chemicals as an Ingredient in Hair Smoothing Products ...
Former FDA Commissioner Dr. Scott Gottlieb joins 'Squawk Box' to discuss the ongoing research and efforts at the FDA to find ...
Food and Drug Administration Commissioner Dr. Marty Makary joins ‘Fox & Friends’ to discuss updated dietary guidelines ...
The U.S. Food and Drug Administration said on Tuesday that it will limit regulation of wearable devices and software designed ...
Certain people risk severe or life-threatening reactions if they consume these products, according to an official alert.
Federal action underscores growing distinction between whole-leaf botanical supplements and synthetic derivatives ...
The FDA classification underscores the urgency of the situation and the potential danger posed by the contaminated products.
After Reviewing Historical Use and Modern Safety Evidence, Officially Confirms Kava is a Food Under Federal Law LOS ANGELES, ...
FDA feedback supports 505(b)(2) filing in H2 2026; No additional studies required beyond current planned 32-subject clinical ...
MedPage Today on MSN
First in-ear EEG device gets FDA clearance
The Naox Link in-ear EEG platform is the first of its kind to be cleared for prescription use at home or in healthcare ...
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