The American Bakers Association has submitted comments to the Food and Drug Administration (FDA) opposing a research proposal to examine how consumers might perceive labeling of added sugars on nutrition labels.
Unilever has begun a voluntary recall of Ben & Jerry’s Chocolate Nougat Crunch Ice Cream in the US, after discovering that allergen advice was missing from the packaging.
The US Food and Drug Administration (FDA) looks set to receive a budget cut of $16.3m for the fiscal year (FY) 2013, despite requesting an additional $253m in funding to boost its Transforming Food Safety Initiative.
The threat of civil litigation is now so great that food manufacturers using any ingredients not found in ‘Grandma’s kitchen cupboard’ should think twice about making ‘all-natural’ claims on pack, according to one firm specializing in food label compliance.
US organic baby formula manufacturer Nature’s One has attacked recent research suggesting that arsenic levels in its toddler formulas were a cause for concern, but the study’s lead author defended the work, even stating that new data published by the...
The firm behind ‘breathable’ caffeine shot AeroShot Energy has promised to amend its marketing to make it clear that it should be ingested – and not inhaled – following a warning letter from the Food and Drug Administration (FDA).
The FDA wrote to the Grocery Manufacturers Association (GMA) and the Food Marketing Institute (FMI) in December in support of the trade groups’ front-of-pack labeling program, saying it would exercise enforcement discretion for certain aspects of the...
The Food and Drug Administration (FDA) is aiming to publish a proposed rule to reform the Nutrition Facts panel and related rules by the end of this year, somewhat later than originally expected.
The US Food and Drug Administration (FDA) has refused to move on allowable levels of carbendazim in orange juice product imports – meeting disapproval from the US industry.
A Brazilian orange juice trade body has called for a stop to ‘double standard’ carbendazim measures after US officials declined to take action against US-manufactured orange juice containing the banned fungicide.
An influential US government office has criticised the US Food and Drug Administration (FDA) for failings in overseeing state food facility inspections, stressing that it paid for inspections that didn’t take place and failed to ensure that ‘systemic...
The US Food and Drug Administration (FDA) must reach a final decision before 31 March 2012 on whether to ban bisphenol A (BPA) in food and drink packaging following the outcome of a lawsuit.
The majority of a $50m increase in Food and Drug Administration (FDA) funding for fiscal 2012 will go toward implementing the Food Safety Modernization Act, after a lobbying group backed by several food industry trade associations played a key role in...
The congressional super committee charged with developing a strategy for deficit reduction has failed to reach an agreement, threatening FDA funding to implement food safety laws, and funding for the 2012 Farm Bill after next year.
We need a formal definition of ‘natural’ to ensure it is used more consistently in food labeling and marketing– and the FDA should provide it - according to the results of the latest FoodNavigator-USA/NutraIngredients-USA poll.
In the world of food marketing, perception is everything. Consumers want foods that sound wholesome, friendly, and above all “natural” – although they are rarely able to articulate what this means.
The Food and Drug Administration (FDA) may have underestimated the risk to pregnant women and children posed by consumption of seafood from the Gulf of Mexico, according to a new risk assessment study.
A study the Food and Drug Administration (FDA) is compiling to determine the level of consumer understanding about whole grains is well-intentioned but could prove to be a waste of time and money unless it is substantially revised, experts have warned.
More than 30 agricultural organizations have signed a letter to Congressional leaders urging them to allow the Food and Drug Administration (FDA) to complete its review of the world’s first genetically engineered fish for human consumption.
A flurry of seizures, criminal charges, and warning letters shows that FDA is increasing it enforcement of dietary supplement regulations. Good for FDA and good for industry!
In an exceptional move, the US Food and Drug Administration (FDA) has issued a statement on the E. coli outbreak gripping Europe, telling American consumers that they do not need to alter their shopping habits.
The Food and Drug Administration has issued its first regulations under the Food Safety Modernization Act – providing stricter control of food imports and giving FDA authority to detain potentially unsafe food.
The FDA is seeking the closure of US juice company Mystical One after it failed to implement an HACCP plan or comply with cGMP requirements and then did not respond to an FDA warning letter.
As genetic testing advances, and commercial tests increase in number, FDA oversight of the tests will strengthen, but it will remain a challenge to not stifle future innovation, says an academic from Duke University.
The Food and Drug Administration (FDA) has issued draft guidance on acidified and fermented foods, such as pickles, relishes and olives, to provide recommendations on manufacturing and quality control.
The problem with Kellogg’s tainted packaging has been solved, US federal authorities said yesterday – as the company confirmed the chemical responsible for the huge recall is not used in its European operations.
The Food and Drug Administration (FDA) should receive full powers immediately to recall food when it threatens health and safety, according to 80 percent of respondents in a telephone survey conducted by Consumers Union Poll.
FDA officials have seized 64 drums of honey imported to the US from China, because it is adulterated with an antibiotic that could cause serious illness or death.
The US food and supplements industry has taken a skeptical stance to a new report that recommends the same scientific approach is used to evaluate health claims on foods and supplements as on drugs and medical devices.
Two more products have been recalled due to the possibility that they may contain salmonella-tainted hydrolyzed vegetable protein (HVP) from Basic Food Flavors – but fears of a large-scale recall have proved unfounded.
A US Congressional watchdog has slammed the Food and Drug Administration (FDA) for a catalogue of failings over its handling of petitions to use irradiation on food.
The Food and Drug Administration (FDA) has met with members of the spice industry to consider ways to make supply safer, following salmonella contamination of salami products linked to black and red pepper.
The FDA needs to improve its oversight of GRAS (generally recognized as safe) food ingredients, claims a new report from the Government Accountability Office (GAO).
In a world with a chronic ‘globesity’ problem spreading beyond western shores to places like India and China, products that promise to help individuals manage their weight via calorie control, fat burning, satiety, or some other mechanism, enjoy rampant...
The International Dairy Foods Association (IDFA) has criticised a planned Food and Drug Administration (FDA) study into front of pack nutrition labels for not having a wide enough scope.
Each day the US Food and Drug Administration (FDA) dithers in delivering its verdict on the safety of bisphenol A (BPA), its authority is diminished and its credibility wanes.
There are serious flaws in a US Government system to help federal agencies pinpoint plants implicated in outbreaks of food-borne illnesses, according to new report.
Tyson Foods has challenged an FDA-assessment that one of its Texas food processing plants had committed “serious violations” of the seafood Hazard Analysis and Critical Control Point (HACCP) regulation.
The US Food and Drug Administration (FDA) has back-tracked on its plans to ban the sale of raw oysters from the Gulf of Mexico during warm months amid mounting industry and political pressure.
Federal agencies in the United States need to increase the speed and accuracy of traceability systems to combat outbreaks of food-borne illnesses, said the FDA as it called a public meeting on the matter.
The US Food and Drug Administration (FDA) is considering issuing guidelines on acrylamide content in food and has published a notice in the Federal Register seeking comments from industry on the issue.
AHD is entering the stevia sweetener market in the US with an extract sourced from Japan; meanwhile, Sweet Green Fields has announced that it has received GRAS notification for its stevia from the FDA.
A notice detailing the new process for issuing warning letters to food companies that violate safety regulations has been published in the Federal Register, with the program due to begin on September 15.
Plainview Milk Products Cooperative of Minnesota has issued a recall of all the instant nonfat dried milk, whey protein, fruit stabilizers, and gums that it has manufactured over the past two years, due to possible salmonella contamination.
The US Food and Drug Administration (FDA) has said it is reviewing its advice that bisphenol A (BPA) is safe for use in baby bottles and food containers, pledging to announce its findings within weeks.
Consumers who choose foods labeled ‘zero trans fats’ could still surpass their recommended daily limit due to FDA rules that allow up to 0.49g of trans fat per serving to be rounded to zero, says spread company Smart Balance.
