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In this bonus episode of Food Safety Matters, recorded live at IAFP's 2025 Annual Meeting in Cleveland, Ohio, we speak to two top officials from FDA’s Human Foods Program (HFP) about the HFP’s current areas of focus—including produce safety and other goals aligned with the “Make America Healthy Again” (MAHA) initiative—as well as the future of the HFP and how food safety culture influences its work.

Western Growers and FDA have signed a Memorandum of Understanding (MOU) to improve fresh produce safety and prevent foodborne illnesses through a new data-sharing framework. The MOU is aligned with the Reagan-Udall Foundation’s recently published Roadmap to Produce Safety report.

In support of the development of a systematic post-market review process for chemicals in the U.S. food supply, FDA has published a new Expanded Decision Tree (EDT) chemical toxicity and risk screening tool, which will help prioritize chemicals for safety evaluation based on their structure and estimated toxicity.

Effective August 4, 2025, FDA is changing its import entry review process for regulated goods from a geographic-based system to a national-based system. Industry must be aware of new communication protocols for the Nationalized Entry Review (NER) program.

FDA and CDC have closed their investigation into a Listeria outbreak linked to ready-to-eat products produced by Fresh and Ready Foods of San Fernando, California, announcing that one of the ten people who fell ill has died. 

FDA and USDA are issuing a joint Request for Information (RFI) to gather information and data to help establish a federally recognized, uniform definition for ultra-processed foods.

FDA is applauding Consumer Brands Association’s (CBA’s) voluntary commitment to encourage U.S. food producers to remove artificial colorants from foods sold in schools by the start of the 2026–2027 school year. CBA said that, while these ingredients are “safe” and “supported by scientific evidence,” the food industry “recognizes preferences are evolving.”

After a nine-month delay, Series 2 of FDA’s and the Alliance to Stop Foodborne Illness’ joint Food Safety Culture Webinar Series will kick off in September.

The Ensuring Safe and Toxic-Free Foods Act of 2025 would set stricter requirements for manufactures to decide a food ingredient is “Generally Recognized as Safe” (GRAS). It also sets an annual quota of GRAS notices for FDA to review, and lays the groundwork for a systematic chemical reassessment process.

In response to FDA’s “Deregulatory Plan,” FMI—The Food Industry Association is urging FDA to make revisions to the “burdensome” Food Traceability Final Rule/FSMA 204, which FDA has already delayed by 30 months.