FDA

Following Infant Formula Incidents, FDA Urges Manufacturers to Implement Stronger, Substantive Supplier Oversight

hendersonb@bnpmedia.com (Bailee Henderson) — Mon, 13 Jul 2026 14:02:02 -0400

The letter to industry was issued in response to the botulism outbreaks linked to Nara Organics and ByHeart formulas, which identified Clostridia in the whole milk powder ingredient supply chain, as well as the global formula recall due to cereulide-contaminated arachidonic acid oil.

FDA Analyzes 15 Years of Mycotoxin Monitoring Data, Finds Low OTA Prevalence

Thu, 09 Jul 2026 05:00:00 -0400

The study represents the first publication of a large FDA dataset on ochratoxin A (OTA) occurrence in U.S. foods. OTA was detected above the limit of detection in 3.5 percent of all samples (which were targeted based on their susceptibility to contamination).

FDA Announces August Public Meeting on Foodborne Listeria monocytogenes Prevention

Wed, 08 Jul 2026 11:41:32 -0400

L. monocytogenes is the fourth-leading foodborne illness-related cause of death in the U.S. Despite continued efforts, listeriosis incidence rates have not declined, prompting FDA to launch a series of public engagements to discuss best practices for managing the pathogen.

FDA to Hire 2,200 Staffers as it Narrows Search for Commissioner, Names Produce Safety Director

hendersonb@bnpmedia.com (Bailee Henderson) — Tue, 30 Jun 2026 12:33:25 -0400

After losing more than 4,000 employees since the Trump Administration took office, FDA is in the process of hiring and re-hiring thousands. The agency is also close to choosing its next Commissioner and has selected a new Director of Produce Safety in the Human Foods Program’s Office of Microbiological Food Safety.

Small-Scale Produce Growers Share Perspectives on FDA’s Produce Safety Rule Exemptions

Tue, 30 Jun 2026 05:00:00 -0400

Researchers from Purdue University conducted focus groups with Indiana produce growers who qualified for exemptions from the Food Safety Modernization Act Produce Safety Rule, examining the beliefs and practical constraints that shape on-farm food safety practices.

FDA Human Foods Program Updates 2026 Guidance Agenda to Include ‘Healthy’ Claim, Caffeine Labeling

Mon, 29 Jun 2026 14:11:23 -0400

The guidance agenda lists topics that the program is considering for possible guidance documents or revisions to existing guidance documents, spanning Food Chemical Safety, Dietary Supplements, and Innovation; Microbiological Food Safety; and Nutrition.

CDC, FDA, USDA Collaboration Defines Framework for Classifying REP Strains, Identifies Strains of Concern

Fri, 26 Jun 2026 05:00:00 -0400

Reoccurring, emerging, and persisting (REP) strains cause foodborne illnesses over extended periods of time, rather than through isolated outbreaks. The REP framework was jointly developed by CDC, FDA, and USDA-FSIS through the Interagency Foodborne Outbreak Response Collaboration.

Food Safety Provisions in the 2026 Farm Bill

hendersonb@bnpmedia.com (Bailee Henderson) — Wed, 17 Jun 2026 05:15:00 -0400

As it stands, the bill would mandate that USDA provide guidance on HACCP plans to small and very small meat processors, require USDA and FDA to define “honey” and establish honey authenticity testing standards, and initiate other directives.

65 Organizations Petition FDA to End Routine Preventive Antibiotic Use in Food Animals

Tue, 16 Jun 2026 15:27:47 -0400

Citing concerns about antibiotic overuse in food-producing animals contributing to the spread of antimicrobial resistance (AMR), the petition calls for FDA to withdraw approvals for the routine use of medically important drugs for disease prevention.

FDA Traceability Rule Readiness Exercises Reveal Supply Chain Coordination Matters More than Technology

Thu, 11 Jun 2026 09:36:36 -0400

A series of tabletop exercises led by FDA and involving food companies across the supply chain revealed industry’s progress and challenges in meeting the requirements of the Food Traceability Rule/FSMA 204.

After Infant Botulism Outbreak, FDA Shares Root Cause Analysis Findings from ByHeart Formula Plants

hendersonb@bnpmedia.com (Bailee Henderson) — Thu, 04 Jun 2026 14:44:19 -0400

FDA did not identify deficiencies in ByHeart’s production facilities that could explain the outbreak, but a powdered milk ingredient did test positive for C. botulinum. ByHeart is developing an action plan based on data generated from the investigations.

FDA Opens Third Salmonella–Moringa Outbreak Investigation of the Year

hendersonb@bnpmedia.com (Bailee Henderson) — Fri, 29 May 2026 06:00:00 -0400

The agency has also reopened a previously closed Salmonella outbreak investigation linked to powdered moringa supplements, with 22 new reported illnesses in four additional states.

FDA Engages Stakeholders on FSMA 204 Implementation With Questions About Lot-Level Traceability

Fri, 29 May 2026 05:30:00 -0400

The agency has released a discussion paper offering context and questions about the lot-level tracking requirements of the Food Traceability Rule to help shape engagements with industry, including a virtual public meeting in June.

FDA Modernizes Oversight of Pesticides in Food

Thu, 28 May 2026 13:13:47 -0400

The updated compliance program for pesticide residues includes a new focus on risk-based sampling of foods commonly consumed by young children and reflects procedural changes to the laboratory testing and analysis methods.

Bipartisan Bill Would Give FDA Authority to Destroy Contaminated Food Imports

hendersonb@bnpmedia.com (Bailee Henderson) — Wed, 27 May 2026 17:19:32 -0400

Highlighting contaminated seafood as a particular concern, the Destruction of Hazardous Imports Act answers FDA’s request for the authority to destroy food imports that do not pass safety inspections at the border, preventing importers from “port shopping” their unsafe products.

FDA Supports Grouping Several Phthalates for Cumulative Risk Assessment

Wed, 27 May 2026 12:19:46 -0400

FDA published a literature review on the eight phthalates currently approved for food contact uses to determine whether they should be considered chemically and/or pharmacologically related for the purpose of cumulative risk assessment.

FDA Issues Guidance on Protein Quality Testing for Infant Formula

Thu, 21 May 2026 15:59:27 -0400

The guidance was developed to help manufacturers and laboratories in the design, conduct, evaluation, and reporting of Protein Efficiency Ratio (PER) studies.

FDA Announces FSMA 204 Compliance Training Through FSPCA

Thu, 21 May 2026 14:30:33 -0400

The Food Traceability Rule training, offered through the Food Safety Preventive Controls Alliance (FSPCA), provides industry participants with foundational knowledge needed to understand and comply with FSMA 204 requirements.

Donald Prater Becomes New Head of FDA Human Foods Program

hendersonb@bnpmedia.com (Bailee Henderson) — Fri, 15 May 2026 13:00:08 -0400

Dr. Prater is taking over the position as the previous Deputy Commissioner for Human Foods, Kyle Diamantas, is elevated to the FDA Commissioner role, replacing Dr. Marty Makary.

Top U.S. Food Safety Officials Discuss Regulatory Landscape at Food Safety Summit

hendersonb@bnpmedia.com (Bailee Henderson) — Thu, 14 May 2026 13:06:25 -0400

On Thursday morning, officials from FDA, USDA-FSIS, CDC, and AFDO took the stage at the 2026 Food Safety Summit Town Hall to talk about the current developments and priorities at their respective agencies.

FDA Encourages Industry to Develop Best Practices, Use Root Cause Analyses

Wed, 13 May 2026 16:30:48 -0400

The agency has released two new web resources to help stakeholders work with FDA as they develop best practices and implement root cause analyses.

FDA Commissioner Steps Down, To Be Replaced by Agency’s Human Foods Leader

hendersonb@bnpmedia.com (Bailee Henderson) — Tue, 12 May 2026 14:15:50 -0400

Marty Makary, M.D., has been ousted as FDA Commissioner. He will reportedly be replaced by the agency’s Deputy Commissioner for Human Foods, Kyle Diamantas, J.D.

FDA Finalizes Systematic Post-Market Food Chemical Review Process

Tue, 12 May 2026 12:55:16 -0400

The agency also announced the launch of reassessments for butylated hydroxytoluene (BHT) and azodicarbonamide (ADA).

New USDA Dietary Guidelines with a Focus on Food Packaging

Fri, 08 May 2026 00:00:00 -0400

This article discusses what the recently released Dietary Guidelines for Americans 2025–2030 say about "highly processed foods" and the food packaging concerns associated with such foods.

FDA Launches One-Day Inspectional Assessments

Wed, 06 May 2026 12:44:25 -0400

Piloting of these assessments began in April and will continue through fiscal year 2026 at facilities across FDA inspectorates, including human and animal foods. The assessments are short, focused screening assignments that complement standard FDA inspections.

Aldi's Decision to Ban 44 Food Additives Gets Ahead of Regulatory Uncertainty

hendersonb@bnpmedia.com (Bailee Henderson) — Fri, 01 May 2026 12:39:08 -0400

Responding to growing consumer and regulatory demand for “natural” foods, the decision builds on Aldi’s removal of 13 synthetic colorants from its portfolio more than ten years ago. The grocer announced this ban while Congress, states, and industry debate ingredient oversight.

Raw Farm E. coli Outbreak Ends; Congress Questions Why FDA Never Used Mandatory Recall Authority

hendersonb@bnpmedia.com (Bailee Henderson) — Thu, 30 Apr 2026 12:45:29 -0400

The E. coli outbreak involving Raw Farm unpasteurized dairy products has ended with one raw cheese sample matching isolates from a different 2025 outbreak. In an April 29 hearing, Congresspeople questioned whether U.S. Health Secretary Kennedy influenced FDA’s failure to mandate a recall.

Federal Preemption of State Food Safety Laws Debated During Congressional Hearing

hendersonb@bnpmedia.com (Bailee Henderson) — Wed, 29 Apr 2026 17:42:08 -0400

In an April 29 Congressional hearing considering 28 active food safety bills, U.S. Representatives and witnesses from industry and consumer protection groups debated federal preemption of state food safety laws, GRAS and chemical ingredient oversight, and FDA–state information-sharing during outbreaks.

FDA Testing Shows U.S. Infant Formula is Safe, with Undetectable or Very Low Chemical Contamination

Wed, 29 Apr 2026 12:00:39 -0400

Samples were tested for arsenic, cadmium, lead, mercury, PFAS, pesticides, and phthalates/plasticizers. When toxic heavy metals were detected in some samples, it was at levels far below EPA drinking water limits.

Bill Reintroduced to Allow FDA to Share Information with State Agencies During Foodborne Illness Outbreaks

Tue, 28 Apr 2026 08:29:48 -0400

The Federal and State Food Safety Information Sharing Act of 2026 would give FDA the authority to share information with state and local regulatory agencies with shared responsibility for protecting public health.