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FDA Announces “Healthy” Claims Consumer Research : On May 6, 2021, the FDA issued a procedural notice on the preliminary quantitative consumer research it plans to conduct on symbols that could be used in the future to convey the nutrient content claim “healthy.”
She was about to have another smoothie as she recovered at home after having her gallbladder removed two days ago when she read an article in the Washington Post about the growing outbreak. Companies – and the FDA and CFIA – have a moral and legal responsibility to protect consumers. FDA, CFIA, what does the public pay you to do?
Based on the doctrine of standing, the Court found that the plaintiff had not shown any ongoing injury sufficient to establish Article III standing. FDA Resumes Domestic Inspections : On July 10, the U.S. Food and Drug Administration announced that it would restart on-site inspections using a new ratings system.
This article focuses on one of the three branches within the newly created U.S. Food and Drug Administration (FDA) Human Foods Program—the Office of Food Chemical Safety, Dietary Supplements, and Innovation—and its potential impact on food packaging.
Food and Drug Administration (FDA) has issued a draft guidance for industry titled “ Recommendations for Collecting Representative Samples for Food Testing Used as Evidence for Release of Certain Fish and Fishery Products Subject to Detention Without Physical Examination (DWPE) and Removal of a Foreign Manufacturer’s Goods from DWPE.”
The purpose of this article is to elaborate on the strategies for effective cost management for these programs and explain why it’s important for restaurant groups to manage their prescription drug expenditure. Strategies that exclude select non-FDA approved products.
On March 5, the FDA issued the final guidance “ Dietary Supplements: New Dietary Ingredient Notification Procedures and Timeframes: Guidance for Industry.” The new guidance is intended to help manufacturers and distributors of NDIs and dietary supplements prepare and submit new dietary ingredient notifications (NDINs) to the FDA.
This article summarizes recent regulatory developments that provide insight on how the current U.S. Concerns around food safety and scalability have surfaced since the successful launch of cultivated meat products in the U.S. regulatory framework addresses food safety within the cultivated meat space.
— OPINION — By Steven Grossman, Executive Director of the Alliance for a Stronger FDA. What started as a crisis over the safety and supply of infant formula became a wide-ranging review of FDA’s food programs by the Reagan-Udall Foundation. We have played a key role in the doubling of FDA’s taxpayer funding. Register her e.
Business owners have 15 days to respond to FDA warning letters. On March 26, 2023, the FDA conducted the business’s Foreign Supplier Verification Program (FSVP). After the inspection, an FDA investigator provided the company with a Form FDA 483a FSVP Observations. 331(zz)).
Unfortunately, we know the FDA will not protect us anytime soon. The FDA told us. In May, the FDA pledged to review chemicals of concern. But, in the same announcement , the FDA said doing so will require more funding and new legal powers. Pledges by the FDA to conduct safety reviews often go unfulfilled.
— COMMENTARY — By Steven Grossman, executive director of the Alliance for a Stronger FDA On Sept. The Alliance for a Stronger FDA had already circulated a shutdown toolkit for FDA stakeholders. FDA still faces a range of outcomes from a modest increase to a devastating cut. The threat was real. 19 and on Jan.
True, perhaps he did not know that his Broken Arrow Plant had Listeria positives going back over years, but knowledge is not necessary for the FDA and a US Attorney to prosecute – just ask the Jensens and DeCosters. Congress passed the Federal Food, Drug, and Cosmetic Act in 1938 in reaction to growing public safety demands.
Jones is scheduled to begin at the FDA on September 24, 2023. I’m delighted to welcome Jim to the FDA. His impressive career, extensive leadership experience, and passionate vision for the future of the Human Foods Program make him an ideal selection for this pivotal position,” said FDA Commissioner Robert M. Califf, M.D.
This article discusses the recent wave of state bills on food additives that have emerged following the California Food Safety Act , FDA’s activities in an effort to get ahead of an inconsistent patchwork of legislation, and criticisms about these bills voiced by legislators, regulators, and industry stakeholders.
This article summarizes the results of the U.S. Food and Drug Administration (FDA’s) Pesticide Monitoring Program Report for fiscal year (FY) 2022, including the rates of violative samples, imported versus domestic foods, and chemicals of concern.
This article will provide insights into restaurant maintenance strategies, best practices to implement them, and tips and tricks to drive long-term success. Proper maintenance is also essential to customer satisfaction, retention, and word-of-mouth reputation building.
Califf, FDA Commissioner of Food and Drugs Last month was the first anniversary of the White House Conference and National Strategy on Hunger, Nutrition, and Health. The FDA continues to make significant progress in our nutrition efforts, which can help combat the diet-related disease epidemic. By: Robert M.
9, 2023, the FDA announced that WanaBana USA had voluntarily recalled three applesauce brands—Weis, WanaBana, and Schnucks—“due to reports of elevated levels of lead.” 8, 2024, the FDA had received 87 confirmed complaints/adverse event reports linked to the recalled product. BACKGROUND : On Nov. As of Jan.
Most recently, FDA released its Draft Guidance for Industry: Action Levels for Lead in Food Intended for Babies and Young Children. This article will discuss the consumer and regulatory drivers of recent years, and also explore the congressional investigation and FDA's subsequent Closer to Zero effort.
The article says the cinnamon originated in Sri Lanka and was shipped to Ecuador, where it was ground into a powder. It was probably there, the FDA has said, that the cinnamon was likely contaminated with lead chromate, a powder that is sometimes illegally used to tint or bulk up spices. The headline is misleading.
In an article Is It Really Expired? While companies aren’t required to put dates on products (except for baby formula), they cannot print false or misleading information — but they also don’t need FDA approval for any dates they do print. Ultimately, expiration dates have much more to do with quality than safety.
Food and Drug Administration (FDA) 2020 Leafy Greens Action Plan was deployed, utilizing sophisticated technologies such as blockchain and machine learning to ensure that people don’t get sick from salad greens. A Food Safety Tech article by Deane Falcone gives an excellent introduction to the problem. coli in the U.S. coli O157: H7.
Food and Drug Administration (FDA) began to include new restrictions in new Food Contact Notifications on the use of food contact substances for infant applications. Recently, FDA has hosted webinars to present information on regulatory requirements and considerations for infant formula ingredients and packaging.
Food and Drug Administration (FDA) established the Coordinated Outbreak Response and Evaluation (CORE) Network to serve as the agency's focal point for response coordination and evaluation of foodborne illness outbreaks. This article explores the evolution, work, and perpetual improvement of the CORE Network.
In an Opinion article , Frank Yiannas, former FDA Deputy Commissioner of Food Policy and Response, urged Newsom to think carefully about the ban, noting that three of the five original ingredients targeted by the California ban are currently under review by FDA. “In
This article examines food recall trends for 2024, including USDA and FDA guidance expanding the scope of recalls and class action lawsuits filed in response to foodborne illness and recall events. The author discusses what these trends mean for industry, and if they are expected to continue into the future.
This article delves into what the new traceability rule means for food manufacturing companies, the operational challenges involved in complying with FDA’s requirements, and how advanced product traceability solutions can help organizations turn compliance into a competitive advantage.
This column explores food processors comments on the potential impacts of important industry developments, including the establishment of FDAs Human Foods Program and USDAs developing new regulatory approach to Salmonella in poultry. The article also delves into processors' priorities for their food safety programs in 2025.
An article this week about Bimbo Bakeries holding off against FDA on an allergen labeling issue. link] Bakery that makes Sara Lee and Entenmann's pushes back on FDA sesame warning by Jonel Aleccia Associated Press October 9, 2024 A top U.S. FDA officials declined to comment, saying they would respond directly to the company.
For example, on the topic of FSQA auditing and inspections, Covid significantly reduced the amount and type of internal and supplier audits as well as FDA inspections. Updates from the FDA and USDA on current projects How to demonstrate Food Safety Culture. Many auditors who were independent contractors just quit.
According to the article in Politico, the "FDA continues to investigate a number of theories for how the pouches became contaminated, and has not drawn any conclusions about the way the lead was added, why or by whom. The FDA says it currently believes the adulteration is “economically motivated.”
Food and Drug Administration (FDA) oversees the safety of food additives and allows only the use of those that are deemed safe. According to expert Charles Spence, in his article On the psychological impact of food color, color is the single most important sensory cue to expectations about the likely taste and flavor of food and drink.
Purchasing gloves with FDA “food compliance” alone may not be a sound food safety strategy. In this article, I provide five key pieces of advice on glove selection and implementation to ensure they remain the foundation of food safety.
This article examines the health risks of PFAS migration from food packaging, and how food and beverage companies can go about phasing out their use to comply with U.S. Food and Drug Administration (FDA) regulations and state laws.
The complaint also stated the Food and Drug Administration inspected the company’s facilities four times, including in 2019, 2020, 2021, and 2022, and that many of the most recent violations were repeat violations the FDA had identified in earlier inspections. Boynton, head of the Justice Department’s Civil Division. Trial Attorney David G.
Well, according to a journal article , Asparagus racemosus (Shatavari) does contain Asparagusic acid, the compound responsible for the asparagus-related pee odor, but this does not seem to be thing (of note).
Allergen-related food recalls have increased since the introduction of FDA's Food Safety Modernization Act in 2011. This article shares the fundamentals of conducting an allergen gap assessment to help companies comply with new FDA guidance on allergen management.
The FDA recently specifically classified gloves as Zone 1 Food Contact Surfaces, meaning in direct contact with ready to eat (RTE) ingredients or finished food products, and at the highest risk for product contamination. however, there is no requirement from the FDA for gloves to arrive “intact, clean, and sanitary” and “impermeable.”
NCA cites its recent litigation in California and the Food and Drug Administration’s (FDA) statement to CR as evidence that chocolate is okay. The Consumer Reports article findings disregard levels previously set by the Superior Court of the State of California, San Francisco County, California in 2018.
Food and Drug Administration (FDA), and the U.S. “This app will be updated as guidelines change, so foodservice can stay up to date on the latest CDC and FDA recommendations.” Hospitality Training Magazine – articles and member blogs with practical training content.
The FDA announced that on Tuesday, March 18, the United States District Court for the District of Maryland entered a consent decree of permanent injunction against Totally Cool, Inc., a Maryland-based manufacturer of ice cream and frozen desserts, and its CEO and owner, Michael J.
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