FDA Seeks Comments on MedSun Device Safety Reporting
Published Date: 7/17/2026
Notice
Summary
The FDA wants your thoughts on how it collects info about problems with medical devices through its MedSun program. This affects hospitals, device makers, and anyone who reports device issues. Comments are open until September 15, 2026, and the FDA aims to keep the process smooth without extra costs or delays.
No Economic Impacts Identified for this Document
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Previous: 2026-14438 — Agency Information Collection Activities; Proposed Collection; Comment Request; Infant Formula Requirements
The FDA wants your thoughts on how they collect info about infant formula rules, like labeling, quality checks, and recordkeeping. This affects infant formula makers who must follow these rules and use a new electronic form to report info. You’ve got until September 15, 2026, to share your comments—no cost changes yet, just a chance to improve how info is gathered!
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The FDA wants your thoughts on a plan to improve how they check if medical products meet safety rules. This affects companies making medical devices and could change how they prove their products are safe. You’ve got until September 15, 2026, to share your ideas—no cost changes yet, just a chance to help shape the process!