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In the waning days of 2022, FDA issued an updated Food Code with several important updates. FDA is responsible for more than a quarter of the U.S. economy, and the Food Code impacts virtually every American. Many of the key changes in the 2022 Food Code relate to food allergens. goes uneaten.
Food and Drug Administration (FDA) announced today it has updated the nutritional requirements a food must meet to use the claim “healthy” on the package, which includes criteria a food must meet to use the healthy claim on the package. For more details, see Use of the Term Healthy on Food Labeling.
Here are the highlights of the Consent Decree : Abbott has agreed to take corrective actions following an FDA inspection of its Sturgis, Michigan facility. Abbott Nutrition will be required to retain an independent expert to review the Sturgis facility’s operations to ensure compliance with the law. In the complaint, filed by the U.S.
When it comes to the term “healthy,” which is a nutrient content claim, the FDA defined it more than 25 years ago in 1993 with a focus on total fats, saturated fat, cholesterol, and sodium. Manufacturers of foods generally considered to be healthy but not low in fat (e.g., Health claims are subject to different FDA rules.
The Reagan-Udall Foundation today announced five members of an Independent Expert Panel who will conduct the operational evaluation of the Food and Drug Administration’s human foods program. Dr. Jane Henney, former FDA Commissioner, was named as Chair of the panel last month.
Over two months ago, while watching the premiere of the documentary, “Poisoned,” at the Tribeca Film Festival in NYC, I got thinking again about how little in the past 30 years I feel I have moved the needle on foodsafety – pathogens and certainly, human nutrition. So, what would I do with a FoodSafety Magic Wand on day one?
Between September 1, 2019 and September 20, 2021, Abbott Nutrition received seventeen consumer complaints regarding multiple Similac powdered formula products. APPLIED – FOI II – BR Abbott Nutritions- FEI# 1815692 9-2021 EIR. The complaint was reviewed by an internal Abbott Nutrition Medical Team. FDA not blameless.
Arkansas Enacts Food Freedom Act : On April 30, 2021, Arkansas enacted the Food Freedom Act that exempts certain producers of homemade foods or drinks products from any state foodsafety licensure, certification, or inspection. The act replaces previous regulations on the cottage food industry.
This review is part of FDA’s “New Era of Smarter FoodSafety: FDA’s Foodborne Outbreak Response Improvement Plan” that also requires a hard look and the support by those concerned about improving the safety of our food and driving the numbers of ill consumers down. Thanks to the deep dive by Craig Hedberg.
HHS, OIG posted this morning: The Federal Food, Drug, and Cosmetic Act requires the Food and Drug Administration (FDA) to safeguard the Nation’s food supply, including infant formula, and ensure that all ingredients are safe. Food and Drug Administration. Office of Audit Services. W-00-22-59472.
Now the question is will Congress and the FDA Commissioner take the recommendations to heart? Most FDA employees understand the immense responsibility of the Agency’s Human Foods Program, appreciate the importance of their work, and share a common value of striving to protect public health.
Validating and verifying foodsafety. AI algorithms are uniquely able to analyze data from various sources, such as FDA inspections, supplier data, and public records, to validate suppliers’ claims and maintain a high level of trust throughout the supply chain.
Food and Drug Administration is announcing an important step to provide nutrition information to consumers by proposing to require a front-of-package (FOP) nutrition label for most packaged foods. Comments on the proposed rule can be submitted electronically to [link] by May 16, 2025.
The FDA and Stop Foodborne Illness are hosting the eighth webinar in the ongoing series of webinars exploring foodsafety culture on September 13, 2023, from 12pm to 1:00pm ET. To learn more about the webinar series and listen to recordings of past webinars, visit Collaborating on Culture in the New Era of Smarter FoodSafety.
In a February 17 resignation letter, James (Jim) Jones, FDA Deputy Commissioner for Human Foods, stated that 89 indiscriminate firings in the Human Foods Program, including layoffs of employees with highly technical expertise in nutrition, infant formula, foodsafety response, would render his job to protect foodsafety fruitless.
A food product is also considered “adulterated” if it bears or contains any poisonous or deleterious substance, which may render it injurious to health. The 1938 Act, and the recently signed FoodSafety Modernization Act, stand today as the primary means by which the federal government enforces foodsafety standards.
On December 6, the FDA and Stop Foodborne Illness will co-host the ninth complimentary webinar in the ongoing series, Collaborating on Culture in the New Era of Smarter FoodSafety.
According to the CDC and FDA, at least 4 kids were sickened and of those two died, from drinking Abbott infant formula. Under the proposed consent decree, Abbott Nutrition will be required to retain an independent expert to review the Sturgis facility’s operations to ensure compliance with the law. Abbott denies the connection.
FDAs leadership webpage was updated this week to include Mr. Diamantas and stated that as the Acting Deputy Commissioner for Human Foods, he leads the agencys Human Foods Program, overseeing all FDAnutrition and foodsafety activities. The post FDA names Kyle Diamantas J.D.
EPA’s James “Jim” Jones was named Wednesday as the first FDA Deputy Commissioner for Human Foods. A Yiannas-Mayne rift was reported in 2022 that was so serious that they’d even argue about how food outbreaks should be investigated. Jones is scheduled to begin at the FDA on Sept. food supply.
The FDA is alerting parents and caregivers about two varieties of LittleOak infant formulas that the company is currently recalling. The products have been sold in the United States illegally because the company has not submitted the required premarket notification to the Food and Drug Administration.
FoodSafety Tech and the American Frozen Food Institute (AFFI) are excited to announce that the 2025 FoodSafety Consortium will be held at the Crystal Gateway Marriott in Arlington, Virginia, from October 19-21. Address current challenges and advancements in foodsafety, technology, and compliance.
based in Oakmont, PA is recalling select lots of NuGo Dark Chocolate Chip and Dark Chocolate Pretzel nutrition bars because they may contain undeclared milk. Brand Name: NuGo Product Description: NuGo Dark Chocolate Chip Nutrition Bar and NuGo Dark Pretzel Chocolate Nutrition Bar Company Announcement FOR IMMEDIATE RELEASE: Jan 10, 2025.
The Independent Expert Panel, charged with generating the report by December 6th, is comprised of researchers, former regulators, and process improvement specialists with disciplinary expertise and experience in epidemiology, food science and safety, microbiology, nutrition, and regulatory operations.
Food and Drug Administration. On November 25, 2024, FDA reported it was was notified about an outbreak of Listeria monocytogenes in the United States, with many ill people residing in long-term care facilities (LTCF) prior to illness onset. Records reviewed from facilities indicated nutritional shakes were available to residents.
Before moving Lucas to palliative care, a PEG tube was operatively inserted into his abdomen so he could be fed without having to use IV nutrition. He continued to have contractures of his extremities and continued medications for that.
Food and Drug Administration has escalated efforts to ensure the safety of infant formula production by issuing warning letters to three major manufacturers: ByHeart Inc., Mead Johnson Nutrition (Reckitt), and Perrigo Wisconsin, LLC. 30, 2023, warning letter, the FDA described a Dec. ByHeart Inc. 21, 2022, through Feb.
Comments received through the Stakeholder Portal will be shared with the Independent Expert Panel charged with generating the recommendations for FDA. On September 29-30 , the Reagan-Udall Foundation will facilitate a public meeting of the Independent Expert Panel on food.
At MenuTrinfo, following FDA guidelines has always been our policy. We take great care to guarantee that our services, training and Certified Free From allergen certifications reflect the most current and accurate allergen information outlined by the FDA as a governing body. What changed as of January 6th, 2025?
The Food and Drug Administration (FDA) has issued a warning about certain tejocote root supplements substituted with toxic yellow oleander. The FDA’s warning has prompted World Green Nutrition, Inc. Tejocotex Amazon.com Alipotec South TX World Green Nutrition, Inc. Additional sample analysis is pending.
The Canadian Food Inspection Agency (CFIA) has issued a foodsafety warning over LittleOak brand infant formula. The company has not submitted the required pre-market submission, these products have not been evaluated to determine whether they meet Canadian foodsafety and nutritional standards and regulations.
In 30 years of practice, I have on numerous occasions offered to FDA leadership the opportunity to meet directly with the people who consumed food that was tainted under the FDA’s watch. He had no meaningful vocalizations and was receiving nutrition through a feeding tube.
That means that restaurants need to work hard to reduce contamination, control pesticide use in high-risk foods, implement rigorous surface sanitation protocols, and adopt sustainable practices to create safer, more responsible dining experiences. Foodsafety professionals should stay informed on updated pesticide regulations.
The Food and Drug Administration, in partnership with STOP Foodborne Illness, a non-profit public health organization, is set to host the eighth installment of its webinar series on foodsafety culture. According to the FDA, foodsafety culture stands as a cornerstone in the FDA’s New Era of Smarter FoodSafety blueprint.
The FDAFoods Coalition was announced Thursday in Washington, D.C., promising to put more pressure on the federal government for improved foodsafety. Califf began his second tour as FDA Commissioner, all sorts of pressures have been applied for change. This has led to a movement to “get the F out of the FDA.”
A senator and representative have introduced legislation that would give the FDA and CDC authority to enter and collect samples at feedlots during foodborne illness outbreaks. coli outbreak investigation, the FDA traced the strain of outbreak E. The FDA also determined that nearby cattle were likely the source of E.
The USDA has appointed 21 new members and nine returning members to the National Advisory Committee on Microbiological Criteria for Foods (NACMCF). The purpose of the committee is to provide impartial scientific advice and recommendations to federal foodsafety agencies. Global Alliance for Improved Nutrition, Washington, D.C.
Food and Drug Administration (FDA) announced today that Bravo Packing, Inc., an animal food manufacturing company of Carney’s Point, New Jersey, has agreed to stop selling, manufacturing and distributing raw pet food and come into compliance with the Federal Food, Drug, and Cosmetic Act (FD&C Act).
The FDA Center for FoodSafety and Applied Nutrition (CFSAN) is hosting a free hybrid public meeting entitled “Modernizing Food and Drug Administration Recalls Listening Session” on September 29, 2023, from 9:00am-5:00pm ET. 1503A (the Great Room), Silver Spring, MD 20993. Virtual registration is also available.
Food and Drug Administration’s (FDA’s) Human Foods Program has published a list of priority work it intends to deliver upon in Fiscal Year 2025, spanning microbiological foodsafety, food chemical safety, and nutrition.
Program areas would include foodsafety, chemical safety and innovative food products, including those from new agricultural technologies, that will bolster the resilience of the U.S. Jones is scheduled to begin at the FDA on September 24, 2023. I’m delighted to welcome Jim to the FDA. Califf, M.D.
ADM Animal Nutrition, a division of ADM (NYSE: ADM), is recalling specific pelleted animal feed products because they may contain elevated levels of copper or have levels of zinc below the represented amounts which could be harmful to cattle. ADM discovered this issue during routine production.
The Food and Drug Administration’s first Deputy Commissioner for Human Foods, Jim Jones, started his work yesterday and sent the below letter to colleagues. FDA Commissioner Robert Calif appointed Jones after the agency’s embarrassing turmoil over the lack of a clear chain of command on the food side of its responsibilities.
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