The Medical Device Recall Improvement Act of 2025 aims to enhance the way medical device recalls are communicated to the public. The main goal is to ensure that notifications about recalls are clear, timely, and accessible, thereby improving patient safety and awareness. Key provisions of the Act include the establishment of an electronic format for recall notifications. Within two years of the law's enactment, the Secretary of Health and Human Services must create a standardized electronic form that manufacturers and importers must use to report recalls.