On December 9, 2025, Texas and Florida filed a new federal lawsuit in the Northern District of Texas aimed at rolling back FDA actions that have kept mifepristone on the market and expanded access over time. The complaint targets the FDA’s original approval and later changes, including policies that widened distribution and enabled mailing of the medication.
For medical professional liability, the immediate “so what” isn’t whether the plaintiffs ultimately win. It’s that this filing keeps reproductive care squarely in a litigation-and-regulation cycle where the rules of engagement can shift faster than clinic operations and physician protocols. When that happens, claim narratives tend to blur clinical decision-making with compliance arguments, especially around documentation, informed consent, follow-up pathways, and how care is delivered across locations and settings.
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