With summer vacation season upon us, most people can relate to the angst of the question, “Are we there yet?” In fact, I suspect many food industry professionals have recently pondered this question when reflecting on the regulations of the Food Safety Modernization Act (FSMA), and then wondered what is “coming down the pike?”
Upon enactment of the FSMA law in January 2011, the U.S. Food and Drug Administration (FDA) implemented a few requirements immediately, but the most significant rules require years to develop. The implementation phase of the FSMA regulations officially began two years ago with the beginning of Phase II of the FDA’s operational strategy for FSMA, which included regulator training and targeted risk-based inspection, sampling, testing and data collection activities. Continue reading Regulatory Round-Up: The Seventh Year of FSMA – Are We There Yet?
Those with lengthy careers or students of food microbiology history may recall the original Listeria Hysteria in the 1980s. While Listeria monocytogenes was responsible for an outbreak associated with fluid milk earlier in the decade, the Jalisco Cheese-related outbreak in 1985 was a major eye opener for the food industry. In the ensuing years, multiple dairy products were found to contain Listeria monocytogenes. A few years after that, the Ready-to-Eat (RTE) meat industry was the center of attention relative to reported incidents of contamination with Listeria monocytogenes. Over the next few years, fruits, vegetables, seafood, deli salads and other products were also found to contain Listeria monocytogenes. Continue reading Technical Tuesdays: Where is Listeria Lurking in The Food Industry?
What is a “healthy” food? Should a “healthy” food contain specific levels of vitamins and minerals? Conversely, should a “healthy” food limit potentially harmful components such as saturated fat, cholesterol, sugar or sodium? Questions surrounding the definition of a “healthy” labeling claim have surged in recent years due to the rising consumer demand for nutritious foods. Continue reading Regulatory Round-Up: What is a ‘Healthy’ Food? – FDA Reconsidering the Definition of ‘Healthy’
A decade ago, allergens were an uncommon cause of meat and poultry product recalls in the United States. The proportion of meat and poultry products recalled annually due to allergens steadily increased from 8% in 2008 to 35% in 2012 due to increased awareness of the issue by inspection personnel and establishments. Moreover, the total number of recall events involving meat and poultry products due to undeclared allergens increased 103% between the calendar years 2012 and 2015. Undeclared allergens have now become the leading reason for recalls of meat and poultry products from the U.S. marketplace. Continue reading Regulatory Round-Up: Keys to Preventing Undeclared Allergens and Reducing Recalls
A majority of consumers find the Genetically Modified Organisms (GMOs) debate complex and confusing, especially with regulations varying from country to country. With the growing push to eat more “all natural” and “organic” foods comes increased concerns about products that are manufactured with genetically modified ingredients, irregardless of concrete evidence that GMOs are either good or bad for human health.
After months of debate in Congress, President Barack Obama signed a bill into law requiring the labeling of food containing genetically modified ingredients on July 29th. To make more sense of the new law, below is a brief list of the main takeaways from the legislation: Continue reading The New GMO Law: 4 Takeaways for Food Manufacturers