FDA

FRESH Act Aims to Preempt State Food Safety Laws, Proposes Controversial GRAS Reforms

hendersonb@bnpmedia.com (Bailee Henderson) — Fri, 24 Apr 2026 14:54:15 -0400

The draft bill proposes sweeping reforms to FDA’s food safety oversight, including GRAS process changes, infant and baby food safety provisions, and federal preemption of state laws. Consumer groups say the FRESH Act’s GRAS reforms and federal preemption language would weaken U.S. food safety.

Congress to Hold Legislative Hearing on 28 Active Bills Related to Food Safety, FDA

Fri, 24 Apr 2026 08:21:16 -0400

The bills to be discussed address issues like “Generally Recognized as Safe” (GRAS) determinations, food chemical safety reassessments, food labeling, infant formula and baby food safety, information-sharing between federal and state agencies, additional FDA authorities for human foods oversight, and other topics.

Tips for Building Confidence in Your Third-Party Laboratory's Salmonella Results

Fri, 24 Apr 2026 00:00:00 -0400

This article reviews why testing for Salmonella is important, the challenges encountered when testing for Salmonella (specifically when using FDA's Bacteriological Analytical Manual Chapter 5 guidelines), and how to evaluate if your testing laboratory is providing reliable testing results.

From Concept to Commercialization: Regulatory Developments Shaping the Cultivated Protein Market

Tue, 21 Apr 2026 10:00:00 -0400

Cultivated protein is moving from concept to commercialization, but a fragmented mix of federal progress, state-level restrictions, and uneven global regulation makes regulatory strategies a key determinant of success.

FDA to Hold Town Halls on Food Traceability Rule Implementation

Thu, 09 Apr 2026 15:19:14 -0400

Registration is now open for the virtual meetings on FSMA 204, which will be jointly hosted with the Partnership for Food Traceability. FDA is interested in hearing stakeholder feedback on lot-level traceability efforts, industry challenges, and potential solutions.

FDA Launches BRIDGE Project to Modernize Food Facility Inspections

Wed, 08 Apr 2026 08:51:15 -0400

Working toward an Integrated Food Safety System, by 2030, FDA expects the Better Regulatory Inspections for Dynamic Government Efficiency (BRIDGE) Project to accomplish a more coordinated, data-driven model for domestic food safety oversight across federal and state systems.

FDA FY 2027 Budget Request Includes $57 Million for ‘MAHA’

hendersonb@bnpmedia.com (Bailee Henderson) — Tue, 07 Apr 2026 14:39:32 -0400

FDA’s Human Foods Program specifically would receive a significant increase in funding compared to the previous fiscal year (FY), including $25 million to help address chemical contaminants and additives like PFAS, toxic heavy metals, and GRAS ingredients.

Stop Foodborne Illness, FDA to Host ‘Culture Change Carnival’ Webinar in April

Mon, 06 Apr 2026 15:34:30 -0400

The free event is open to the public and is the fifth installment in the joint multi-part webinar series focused on advancing food safety culture.

FDA’s Human Foods Program Publishes Priority Scientific Needs to Advance Food Safety

Thu, 02 Apr 2026 14:57:11 -0400

The list of data, method, and research needs spans microbiological and chemical safety, nutrition, risk assessment, and other areas. It is intended to guide researchers who are interested in pursuing impactful food safety research.

Latest FDA Post-Investigation Summary for Mango Salmonella Outbreak Redacts Key Details

hendersonb@bnpmedia.com (Bailee Henderson) — Thu, 02 Apr 2026 08:30:50 -0400

Redacted details include the importer of the implicated mangoes, the country in which the mangoes were grown, and the number and names of states in which outbreak cases were reported.

Drug-Resistant Salmonella Outbreak Linked to Moringa Supplements Ends, Root Cause Remains Unknown

Wed, 01 Apr 2026 16:09:57 -0400

Although FDA was unable to find a cause of contamination, a single supplier of the contaminated moringa powder was identified. Affected products, which were sold under the Rosabella brand and distributed by Ambrosia Brands LLC, have been recalled.

FDA Issues RFI on Changing Market Name for Certain Rockfish to ‘Snapper’

Tue, 31 Mar 2026 15:18:40 -0400

Industry members have requested the market name for specific Sebastes (rockfish) species be changed to “snapper” in the Seafood List. FDA has identified critical areas that must be considered before this change is made, including classification, food safety and hazard identification, and labeling and allergen concerns.

NEHA–FDA Retail Program Standards Symposium to Take Place in April

Mon, 30 Mar 2026 15:58:58 -0400

The free, virtual event for state, local, tribal, and territorial jurisdictions will deliver practical insights on advancing retail food safety in compliance with FDA’s Voluntary National Retail Food Regulatory Program Standards.

IFSAC Publishes Latest U.S. Foodborne Illness Source Attribution Estimates

Fri, 27 Mar 2026 13:11:07 -0400

The Interagency Food Safety Analytics Collaboration (IFSAC) is a joint effort between CDC, FDA, and USDA-FSIS. The latest report covers the year 2023 and focuses on the food vehicles of illnesses from Salmonella, E. coli O157, and Listeria monocytogenes.

Patient Count in Raw Farm E. coli Outbreak Grows, Majority are Young Children

Fri, 27 Mar 2026 09:42:55 -0400

Nearly all of the ill people interviewed reported consuming Raw Farm-brand raw dairy products. Testing and an onsite inspection of Raw Farm’s operation in California is ongoing. Raw Farm LLC has yet to issue a recall.

FDA Delays Approvals for ‘Natural’ Food Dyes Due to Stakeholder Objections

hendersonb@bnpmedia.com (Bailee Henderson) — Wed, 25 Mar 2026 05:30:00 -0400

The delays give the agency time to respond to comments made on the final orders approving beetroot red and spirulina extract for use as color additives in human foods. However, FDA stands by its determinations that the colorants are safe for their intended uses.

Amid E. coli Outbreak, Congress Urges FDA to Mandate Raw Cheese Recall

hendersonb@bnpmedia.com (Bailee Henderson) — Mon, 23 Mar 2026 10:27:00 -0400

“If mandatory authority needs to be strengthened, the Food Safety Caucus stands ready to tackle this issue at FDA’s request,” wrote Congress members in a statement about the ongoing E. coli outbreak involving Raw Farm raw cheese products. Raw Farm has so far refused to recall.

FDA Withdraws COVID-Era Temporary Guidances for Onsite Visits Under FSMA

Wed, 18 Mar 2026 11:51:25 -0400

As COVID-19 no longer significantly impacts travel, FDA believes the temporary guidances are no longer relevant. The withdrawals will be effective on June 16, 2026.

FDA Highlights Successful Mexico-U.S. Effort to Eliminate Salmonella Outbreaks from Papayas

Wed, 18 Mar 2026 06:00:00 -0400

No U.S. Salmonella outbreaks linked to Mexican papayas have been identified since 2020 thanks to collaborative efforts between regulators and industry in both countries. The case study could serve as a framework for improving food safety in other commodities and global supply chains.

Salmonella Outbreak Linked to Moringa Supplements Ends with 97 Sickened in 32 States

Wed, 18 Mar 2026 05:30:00 -0400

The products have been recalled, but have a long shelf life. FDA previously reported working with the manufacturers to determine the root cause of contamination, but has not shared an update at the time of the investigation’s close.

FDA Releases Report Summarizing Foodborne Illness Outbreak Investigations in 2024

Tue, 17 Mar 2026 14:51:51 -0400

The agency’s Office of Coordinated Outbreak Response, Evaluation, and Emergency Preparedness (CORE+EP) evaluated 72 incidents, initiated 26 response investigations, and issued ten public health advisories in 2024.

Multistate E. coli Outbreak Likely Caused by Raw Cheese, but Manufacturer Refuses to Recall

Mon, 16 Mar 2026 10:25:00 -0400

A total of seven patients—four of whom are three years of age or younger—have been sickened in three states. Epidemiologic evidence indicates that RAW FARM-brand unpasteurized cheddar cheese products are the likely vehicle of illness, but product testing is ongoing.

New FDA Risk Assessment Informs FSMA Requirements for Raw Manure Use on Produce

Thu, 12 Mar 2026 13:08:47 -0400

Providing evidence for potential Produce Safety Rule standards, the assessment examined how pathogens survive in untreated biological soil amendments of animal origin (BSAAO) and contaminate produce. FDA found that longer time between BSAAO application and harvest significantly reduces crop contamination.

Congressional Bill Would Direct FDA to Enforce Stronger Infant Formula Safety Oversight

Thu, 12 Mar 2026 10:05:38 -0400

The Infant Formula Safety Modernization Act includes provisions about expanded pathogen testing requirements and compulsory environmental monitoring for infant formula manufacturers, among other mandates.

FDA to Replace Human Foods Complaint System with New Dashboard for All Regulated Products

Wed, 11 Mar 2026 14:05:39 -0400

By the end of May, complaint systems for all FDA-regulated products, including human and animal foods, will be replaced by the new, streamlined Adverse Event Monitoring System (AEMS).

FDA Redacts All Key Details in Summary of Fatal Listeriosis Outbreak Linked to Produce

hendersonb@bnpmedia.com (Bailee Henderson) — Fri, 06 Mar 2026 11:08:19 -0500

Despite having Listeria-positive samples that matched the outbreak strain via whole genome sequencing (WGS), which prompted an FDA Import Alert and a company recall for the suspected vehicle of illness, FDA did not disclose the specific product or any of the firms implicated.

FDA Releases Initial Findings from Foodborne Pathogen Study in California Growing Region

Thu, 05 Mar 2026 16:01:39 -0500

The California Longitudinal Study, a five-year environmental study of California’s Central Coast produce-growing region, identified wildlife, livestock, and surface water as potential contributors to the persistence and movement of Shiga toxin-producing Escherichia coli (STEC).

RFK Jr. Says Federal Ultra-Processed Foods Definition is Coming in April

hendersonb@bnpmedia.com (Bailee Henderson) — Wed, 04 Mar 2026 09:59:13 -0500

In his remarks on a recent Joe Rogan Experience podcast episode, Secretary Kennedy also suggested FDA is considering a new approach to front-of-pack nutrition labeling.

FDA to Hold Public Meeting on Scope of Dietary Supplement Ingredients

Tue, 03 Mar 2026 16:45:23 -0500

The March 27 hybrid event will discuss new methodologies to produce existing dietary ingredients and specific ingredient types, including proteins, enzymes, and microbials, within the scope of the Dietary Supplement Health and Education Act of 1994.

Investigation Identifies More than 100 GRAS Ingredients Used in Foods Without FDA Notification

hendersonb@bnpmedia.com (Bailee Henderson) — Tue, 03 Mar 2026 11:39:36 -0500

Of the 111 “Generally Recognized as Safe” (GRAS) additives identified by the Environmental Working Group (EWG), 49 are known to be widely used by food manufacturers.

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