HRES 803 United States House · 119th Congress

Urging the Director of the Food and Drug Administration to reevaluate the safety of all chemical abortion drugs in light of recent independent studies, and for other purposes.

HRES 803 is a non-binding resolution urging the FDA to reassess the safety of all chemical abortion drugs based on recent independent studies. It specifically requests the FDA reevaluate safety data and publicly release a full safety review including real-world complications. The resolution does not change laws or create new requirements but asks the FDA to consider findings that claim complication rates are 22 times higher than current reports. This resolution directly addresses the FDA's regulatory oversight of these drugs, not other entities or policies.
Bill status in committee 1 of 4 stages cleared
Introduction
Oct 2025
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Introduced Oct 10, 2025 Last action Oct 10, 2025
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Oct 10, 2025
Committee
Referred to the House Committee on Energy and Commerce.
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1 primary · 11 co-sponsors

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