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SQF Edition 10 Releases Early March 2026

By Food Safety Tech Staff
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In early March, SQFI will release the SQF Edition 10 Code, marking an important evolution of the program shaped by extensive industry input.

Edition 10 strengthens audit credibility, reinforces foundational food safety controls, and supports greater confidence in certification outcomes across the supply chain.

Following release, the Code will move through the Global Food Safety Initiative (GFSI) benchmarking process, with a planned transition period to support consistent implementation across the SQF system.

Pending completion of the review process, SQFI anticipates the first Edition 10 audits could begin as early as January 2027 (approximately nine months after release).

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Allergen Alley

FDA Takes Steps to Improve Gluten Ingredient Disclosure in Foods

By Food Safety Tech Staff
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The U.S. Food and Drug Administration issued a Request for Information (RFI) regarding labeling and preventing cross-contact of gluten in packaged food. The FDA is taking this action as a first step to improve transparency in disclosures of ingredients that impact certain health conditions, such as gluten for those with celiac disease, and other established food allergens.

The agency is seeking information on adverse reactions due to “ingredients of interest” (i.e., non-wheat gluten containing grains (GCGs) which are rye and barley, and oats due to cross-contact with GCGs) and on labeling issues or concerns with identifying these “ingredients of interest” on packaged food products in the U.S.

The agency has received a citizen petition on this matter and has reviewed available data and reports including the most recent reports by the Food and Agriculture Organization of the United Nations expert consultation. The FDA’s review of this information indicates that there are several serious data gaps limiting the agency’s ability to fully evaluate the public health importance of these ingredients which includes limited U.S. data on adverse reactions to the “ingredients of interest.”

The FDA seeks detailed information such as the prevalence of products where rye or barley are not currently disclosed; information on the severity of and potency of immunoglobulin E-mediated food allergy to rye and barley; concerns around the gluten content of oats due to cross-contact and other questions related to these issues.

The FDA is taking this action to help enhance transparency for consumers and inform the agency’s gluten-related labeling priorities and next steps. The FDA intends to use the information to support a determination on what type(s) of future regulatory actions we should take to better protect consumers with celiac disease.

How to Submit Comments

Electronic Submissions Comments can be submitted via the Federal eRulemaking Portal to Docket No FDA-2023-P-3942 (open for 60 days). Follow the instructions for submitting comments.

Written Submissions Written comments may be mailed to:
Dockets Management Staff (HFA-305)
Food and Drug Administration
5630 Fishers Lane, Rm. 1061
Rockville, MD 20852

Ensure that all comments include Docket No. FDA-2023-P-3942. Confidential submissions should be appropriately marked.

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Beltway Beat

DeLauro, Durbin Reintroduce the Federal Food Administration Act

By Food Safety Tech Staff
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On December 10, 2025, Congresswoman Rosa DeLauro (CT-03) and Senate Democratic Whip Dick Durbin (D-IL) reintroduced the Federal Food Administration Act, legislation that would streamline our food safety system by consolidating food oversight into a single agency dedicated to keeping the foods Americans eat safe.

“We need a single food safety agency to ensure the food Americans eat is safe,” said DeLauro. “Currently, food safety oversight is scattered across multiple agencies with the bulk of the responsibility falling to the Food and Drug Administration – where food safety has often been treated like a second-class citizen. This legislation would put one agency clearly in charge with the singular mission of protecting our food supply with the resources, staff, and focus to achieve that goal. I am proud to partner with Senator Durbin in this effort, because Americans deserve peace of mind that the government is keeping companies accountable with clear, consistent safety standards.”

“The sad reality is that FDA has failed to protect Americans from preventable foodborne illnesses and death. In recent years, the FDA has failed to protect babies from bacterial infections in their infant formula and lead-tainted applesauce pouches,” said Durbin. “This is why Congresswoman DeLauro and I are introducing legislation to create a Federal Food Administration.  With the Federal Food Administration Act, we hope our nation will have greater success in protecting the foods in our kids’ lunch boxes and on our dining room tables.”

FDA regulates approximately 80 percent of our food supply. Consumers and companies depend on FDA to perform its regulatory role effectively.  Yet, despite increased authorities included in the Food Safety Modernization Act (FSMA) and the creation of the Human Foods Program at FDA, the agency has failed to make significant inroads in reducing rates of foodborne illness and death in the U.S.

About one in six Americans—or 48 million people—get sick from a foodborne illness each year.  According to the Centers for Disease Control and Prevention (CDC), 128,000 Americans also are hospitalized and 3,000 Americans die of foodborne diseases each year.

A single food safety agency, with a Senate-confirmed Commissioner, will strengthen oversight of the food supply, improve the health and well-being of Americans, and ensure companies that cut corners on food safety are properly held accountable.

Joining Durbin and DeLauro as original cosponsors of this legislation is Sen. Richard Blumenthal (D-CT) and U.S. Representative Sara Jacobs.

The legislation is endorsed by Consumer Reports, Consumer Federation of America, Environmental Working Group, and STOP Foodborne Illness.

Apply for IAFNS Emerging Leaders Award for Food Safety and Nutrition Science

By Food Safety Tech Staff
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Open to U.S. and Canadian professionals with less than 8 years of experience since completing their degree, the award includes $2,000 in unrestricted cash and an all-expenses paid trip to Washington DC for IAFNS Annual Summer Science Symposium at the National Press Club. Winners will be awarded a speaking slot at the symposium to share their insights and accomplishments and receive their plaque.

Self-nominations are welcome. Applications will be judged on the applicants’ research, communication, leadership and collaboration skills and accomplishments. We encourage all young researchers and professionals to learn more about this opportunity, which is geared toward recognizing emerging leaders.

One award will be for food safety and another for nutrition. Qualifications include employment in academia, industry or government with a primary role as a researcher in the area of food safety or nutritional sciences. This award is intended for U.S. or Canada-based researchers. The nominees, as of January 1, 2026, must have received their highest graduate degree (M.S. or Ph.D.) in a related field within the previous 8 years.

Important Dates:

Application Opens: January 5, 2026

Application Closes: February 13, 2026, 11:59 PM ET

Award Winners notified: Approximately March 23, 2026

Award presentation at IAFNS Annual Summer Science Symposium: June 24-25, 2026.

As an organization, IAFNS drives, funds and leads actionable science to advance food and nutrition science in support of public health. Please apply today and share with your colleagues who may be interested in this prestigious recognition.

Learn more about the Emerging Leaders Award here.

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Beltway Beat

USDA FSIS Announces Leadership Changes

By Food Safety Tech Staff
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On January 9, 2026, FSIS announced strategic leadership changes that reflect the agency’s goal of ensuring representation, collaboration and accountability at the most senior level of the agency.

Mr. Robert Bane will be joining FSIS’ Office of the Administrator as Deputy Administrator of Field Operations, serving alongside Deputy Administrator Dr. Denise Eblen, who will focus on FSIS’ science and policy work. Bane brings decades of experience and expertise to this position and has served in several leadership positions within FSIS. Most recently, he was Executive Associate for Regulatory Operations within the Office of Field Operations (OFO) and prior to this was Assistant Administrator of the Office of Investigation, Enforcement and Audit. Bane will continue working from the Springdale District Office.

Additional leadership changes were made in OFO, the Office of Management (OM), and the Office of Public Affairs and Consumer Education (OPACE). Ms. Melissa Moore has been named Assistant Administrator of OFO, Ms. Natalie Duncan has assumed the role of Assistant Administrator of OM, and Ms. Karen Hunter has transitioned from her role as Acting Deputy Assistant Administrator of OFO to become the Assistant Administrator of OPACE

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Beltway Beat

FDA Opens VQIP Application Portal for FY2027

By Food Safety Tech Staff
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The FDA’s Voluntary Qualified Importer Program (VQIP) application portal for fiscal year 2027 opens on January 1, 2026, providing food importers with an opportunity to streamline their import processes through expedited review and importation benefits.

VQIP is a voluntary, fee-based program that offers expedited review and importation benefits for human and animal foods when importers demonstrate control over their supply chain safety and security. To participate, importers must ensure their foreign supplier facilities are certified through FDA’s Accredited Third-Party Certification Program.

Key Application Details:

• Application Window: January 1 – September 1, 2026

• Program Year: FY2027 benefits

Getting Started:

• Create an account on the FDA Industry Systems website (https://www.access.fda.gov/)

• Contact FSMAVQIP@fda.hhs.gov for an informational meeting

• Review eligibility requirements and certification needs, as foreign supplier facilities must be certified by FDA-accredited third-party certification bodies.

VQIP supports FDA’s Strategy for the Safety of Imported Food by incentivizing importers to use certified suppliers and maintain robust processes to help ensure imported food meets U.S. food safety requirements.

Resources and Support:

For questions or assistance, contact the VQIP Importers Help Desk:

• Email: FSMAVQIP@fda.hhs.gov

• Phone: 301-796-8745

• Program Information: https://www.fda.gov/food/importing-food-products-united-states/voluntary-qualified-importer-program-vqip

EAS Consulting Group Announces Hiring of Business Development Director Rob Williams

By Jessica Lloyd
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EAS Consulting Group, a company focused on regulatory compliance for FDA- and USDA-regulated industries, is pleased to welcome Rob Williams to the EAS team as Business Development Director.

Rob is an accomplished business development executive with over a decade of experience driving sales growth, strategic partnerships, and market expansion across the healthcare and life sciences industries. In his role with EAS Consulting Group, Rob will support client engagement and growth initiatives across all FDA-regulated commodity areas, helping organizations identify and implement the regulatory and compliance solutions best suited to their needs.

Prior to joining EAS, Rob held key leadership roles in the medical technology sector, including Regional Sales Manager for Neocis, a pioneer in robotic dental surgery, and Senior Portfolio Business Development Manager for Pacira BioSciences, where he led opioid-free pain management initiatives throughout the Mid-Atlantic region. His achievements at Pacira included multiple top national rankings, including #1 for total revenue in several quarters and recognition among the top 10% of the national sales force.

Earlier in his career, Rob served in business development roles with Merit Medical Systems, Lumenis, and Oxford Immunotec, where he consistently exceeded growth targets and formed strategic partnerships with leading healthcare institutions such as Johns Hopkins, INOVA Health System, and Walter Reed National Military Medical Center.

Rob is recognized for his strategic approach to client engagement, leadership in collaborative business development environments, and commitment to advancing innovative healthcare solutions. His work at EAS will further strengthen support for clients navigating evolving regulatory and quality compliance expectations.

Follow Rob on LinkedIn

Beltway Beat

FDA Takes Action to Improve Recall Effectiveness

By Food Safety Tech Staff
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In a December 15, 2025 press release, the U.S. Food and Drug Administration reminded industry of its legal responsibilities under the Federal Food, Drug, and Cosmetic Act regarding food recalls and called for industry to increase adoption of best practices in recall implementation.

Last week, the FDA sent warning letters to several major retailers for failing to remove recalled ByHeart infant formula from their store shelves despite being notified of the recall. These warning letters highlight a concerning problem with recall effectiveness at the retail level. Last year, the FDA sent a similar warning letter to a retailer who failed to adequately remove recalled lead-contaminated WanaBana apple cinnamon fruit puree pouches from its store shelves.

In the weeks following the manufacturer’s voluntary recall of ByHeart infant formula products, FDA investigators and state and local partners checked retail stores across the U.S. over 4,000 times to ensure recalled product was not being made available to consumers. The investigation discovered recalled infant formula continued to be found on store shelves—for over three weeks in one case, in over 175 locations across 36 states. These warning letters highlight the critical responsibility that retailers have in effectuating a recall, particularly when dealing with products that pose serious health risks to our most vulnerable populations, such as infants.

The FDA has asked these retailers to respond to the warning letters within 15 days stating the specific steps they have taken to address any violations and prevent the recurrence of violations, or providing its reasoning and supporting information as to why the company believes it is not in violation of the law.

Cows, dairy, farms

Pasteurization of milk is an Effective Preventive Measure against Avian Influenza

By Food Safety Tech Staff
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Cows, dairy, farms

In March 2024, a highly pathogenic avian influenza H5N1 (HPAI) clade 2.3.4.4b virus was identified in US dairy cows, with spillover to cats, poultry, and humans.

Up to 30% of commercial pasteurized milk tested contained viral genome copies. The impact of residual viral remnants on host immunity is unknown. Orally ingested proteins can stimulate gut-associated lymphoid tissues, potentially inducing tolerance and altering responses to later infection.

The research published by NIH found that milk pasteurization fully inactivated pandemic H1N1 and bovine H5N1 influenza viruses yet preserved hemagglutinin (HA) protein integrity. In mice, repeated oral exposure to inactivated virus did not alter mortality after H5N1 virus challenge.

Preliminary data showed that naïve mice exposed to improperly pasteurized milk containing live H5N1 virus developed lethal infection, whereas prior H1N1 infection conferred protection. Mice with preexisting H1N1 immunity remained protected when challenged with bovine H5N1 virus after exposure to H5N1 pasteurized in milk.

These findings suggest that pasteurized milk containing inactivated H5N1 virus poses minimal health risks.

 

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Beltway Beat

FDA Expands Artificial Intelligence Capabilities with Agentic AI Deployment

By Food Safety Tech Staff
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