Mandatory Cosmetics Recalls Take Shape as FDA Publishes New Q&A Guidance
The U.S. Food and Drug Administration (FDA) has published guidance dated October 2026 that explains how it will use its
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October 23, 2026
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FDA Issues Guidance Exempting Certain Unclassified Medical Devices from 510(k) Premarket Review
The U.S. Food and Drug Administration has released guidance clarifying regulatory expectations for unclassified medical devices and 510(k) premarket notification requirements, formally
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July 3, 2026
What FDA’s New Letter Means for “No Artificial Colors” Food Claims
In a letter issued February 5, 2026, the U.S. Food and Drug Administration (FDA) said it intends to exercise enforcement
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February 8, 2026