by Marion Nestle

Search results: single food agency

May 23 2023

U.S. Nutrition Monitoring System is at Grave Risk

Here’s one of the most important—and alarming—papers I’ve seen in a long time.

Critical data at the crossroads: the National Health and Nutrition Examination Survey [NHANES] faces growing challenges

In summary, NHANES is at crossroads. Its many past successes are impressive, given the ambition of its goals and the complex nature of the data it has been designed to collect. However, the effect of years of inflation on the survey’s stagnant budget has undercut activities to meet the future, and the potentially game-changing nature of newer challenges cannot be avoided. A NASEM study to set the stage for the future of NHANES—that is, to provide an actionable framework—is a critical and prudent step forward. Certainly, maintaining the status quo and failing to adapt to emerging challenges cannot be an option for a survey vital to the nation’s health.

The National Nutrition Monitoring and Related Research Act of 1990 established a system for tracking diet and health in the United States.  Its passage was a long time coming and a terrific step forward.

The Act legally established the National Nutrition Monitoring and Related Research Program and numerous activities including development and implementation of a Ten-Year Comprehensive Plan and formation of the Interagency Board for Nutrition Monitoring and Related Research. Both requirements serve as the basis for planning and coordinating the activities of 22 Federal agencies that either conduct nutrition monitoring surveys and surveillance activities or are major users of nutrition monitoring data.

It set up the data collection system for What We Eat in America and the National Health and Nutrition Examination Survey (NHANES), Originally, the surveys were done by separate agencies, but they are now integrated under the CDC. 

It’s hard to overstate their importance.  Here’s a short list of how what the data are used for:

Everything we know about diet and health—and trends—in the U.S. comes from these surveys.

The report makes it clear that:

  • The CDC has been letting the surveys slide.
  • They are badly underfunded.
  • Nobody is paying attention to them.
  • They are not able to collect the data they need.
  • They are not being revised or modernized to collect new kinds of data.
  • They do not have champions in the public or in government.

I remember what it took to get the 1990 act: concerted efforts from advocacy groups and government nutrition personnel, and a series of reports over a ten-year period.  

Do we need to go through all that again?  It sure looks that way.

The paper calls for a deep investigation of the nutrition monitoring system.

the single most effective action at this time would be an overall and integrated examination of NHANES in the context of its future. Without a well-informed and defined set of goals and recommendations, there cannot be meaningful progress. Such a study would need to not only carry the gravitas of diverse experts with experience and knowledge related to health surveys and to health and nutrition data collection but also provide an independent and consensus-driven report.

That seems like a bare minimum.  Let’s get to it right away.

Mar 2 2023

Keeping up with cell-based cultured meat

I don’t know about you but I’m riveted by what’s in the pipeline for cell cultured meat alternatives.   Here are some recent items I’ve been collecting.

Products under development

State of the industry

State of the techno-food scene

Comment

Cell-based meat, meat-plus-algae, and pet food are not yet on the US market so it’s too early to see what they taste like and how well they will do.  I see these products as mostly about mergers, acquisitions, and generating lots of money for investors, which is why I included the Soylent event (Soylent is a nutrient supplement drink, but I put it in the same category of “techno-food”).

Oct 27 2022

USDA aims to reduce Salmonella in poultry products: a good first step

The USDA is at long last giving some attention—a small but significant first step—to reducing Salmonella contamination of poultry products.

Salmonella is a big problem in poultry and eggs.  For decades, food safety advocates have called on the USDA to declare Salmonella an adulterant.  Adulterated food is illegal to sell.

The poultry industry has resisted, arguing that chicken gets cooked before it is eaten; cooking kills Salmonella.

It does, but you don’t want toxic forms of Salmonella in your kitchen where they can get into other foods.  For background all this, see my book, Safe Food: The Politics of Food Safety.

In a press release, the USDA’s Food Safety and Inspection Service (FSIS) announces that it

is considering a regulatory framework for a new strategy to control Salmonella in poultry products and more effectively reduce foodborne Salmonella infections linked to these products…The most recent report from the Interagency Food Safety Analytics Collaboration estimates that over 23% of foodborne Salmonella illnesses are attributable to poultry consumption—almost
17% from chicken and over 6% from turkey.

The proposed Salmonalla framework has three components:

What FSIS is actually doing:

We will publish a proposed notice of determination to declare Salmonella an adulterant in NRTE [not ready to eat] breaded and stuffed chicken products in 2022, and we intend to publish additional proposed rules and policies implementing this strategy in 2023, with the goal of finalizing any rules by mid-2024.

The adulterant consideration only applies to breaded and stuffed chicken or turkey products that are likely to be microwaved but not necessarily thoroughly cooked.  It does not apply to plain, unbreaded and unstuffed poultry.

Consumer Reports finds lots of poultry to be contaminated with Salmonella.  Consumer Reports says Salmonella is “lethal but legal.”

Currently, a chicken processing facility is allowed to have salmonella in up to 9.8 percent of all whole birds it tests, 15.4 percent of all parts, and 25 percent of ground chicken. And producers that exceed these amounts are not prevented from selling the meat. If salmonella became an adulterant, even in some poultry products, it would help reduce the amount of contaminated meat that hits the market.

As might be expected, the National Chicken Council opposes the USDA’s proposed framework: “lacks data, research.”

the facts show that the Centers for Disease Control and FSIS’s own data demonstrate progress and clear reductions in Salmonella in U.S. chicken products.  “Increased consumer education about proper handling and cooking of raw meat must be part of any framework going forward…Proper handling and cooking of poultry is the last step, not the first, that will help eliminate any risk of foodborne illness. We’ll do our part to promote safety.”

In other words, the poultry industry wants you to be responsible for protecting yourself against Salmonella.  If only you would do a better job of handling and cooking raw chicken.  It does not want to have to reduce Salmonella in its flocks in the first place (something quite possible, by the way).

This is a good first step.  Let’s urge the USDA to go even further and declare Salmonella an adulterant on all poultry sold in supermarkets.

And maybe require poultry producers to do everything possible to prevent Salmonella geting into flocks in the first place.

This won’t be easy, according to a United Nations report from a recent expert meeting.

The expert consultation noted that no single control measure was sufficiently effective at reducing either the prevalence or the level of contamination of broilers and poultry meat with NT-Salmonella spp. Instead, it was emphasized that control strategies based on multiple intervention steps (multiple or multi-hurdle) would provide the greatest impact in controlling NT-Salmonella spp. in the broiler production chain.

The experts concluded that all of the following approaches were needed:

  • Biosecurity and management
  • Vaccination
  • Antimicrobial
  • Competitive exclusion/probiotics
  • Feed and water
  • Bacteriophage (bacterial viruses)
  • Processing and post-processing interventions

***********

For 30% off, go to www.ucpress.edu/9780520384156.  Use code 21W2240 at checkout.

 

 

 

Oct 11 2022

More on FDA’s proposed definition of “healthy”

Last week, STAT News asked if I would write something about the FDA’s definition of “Healthy” for them.  I agreed because I was planning a blog post on it anyway (posted here).

I wrote a draft and had a great time working with a STAT editor, Patrick Skerritt, to fill in some missing pieces.  Here’s how it came out (with a couple of after-the-fact embellishments).

First Opinion: FDA’s plan to define ‘healthy’ for food packaging: Better than the existing labeling anarchy, but do we really need it?   STATNews, Oct. 7, 2022

The FDA has announced the set of rules it proposes to enforce for manufacturers to claim that a food product is “healthy.” The proposed rules are a lot better than the labeling anarchy that currently exists. But here’s my bottom line: health claims are not about health. They are about selling food products.

The FDA says that a “healthy” product must meet two requirements: It must contain a meaningful amount of food, and it must not contain more than certain upper limits for saturated fat, sodium, and added sugars.

To illustrate the “healthy” claim, the FDA is also researching a symbol that food makers can use, and might be testing examples like these.

[Source: https://www.regulations.gov/document/FDA-2021-N-0336-0003]

Doing all this, the FDA says, would align “healthy” with the 2020-2025 Dietary Guidelines for Americans and with the Nutrition Facts label that is printed on food packages.

This action is the latest in the FDA’s attempts to simplify food label information so it’s easier for consumers to identify healthier food choices. It is also an attempt to head off what food companies most definitely do not want: warning labels like those used in ChileBrazil, and several other countries. These have been shown to discourage purchases of ultra-processed “junk” foods, just as they were supposed to, a message understood even by children or adults who cannot read. No wonder food manufacturers will do anything to prevent their use.

If we must have health claims on food packages, the FDA’s proposals are pretty good. They require any product labeled “healthy” to contain some real food (as opposed to a collection of chemical ingredients or, as author Michael Pollan calls them, “food-like objects”), and for the first time they include limits on sugars.

Here’s an example given by the FDA: To qualify for the “healthy” claim, a breakfast cereal serving would need to contain at least three-quarters of an ounce of whole grains and could contain no more than one gram of saturated fat, 230 milligrams of sodium and 2.5 grams of added sugars.

These proposed rules would exclude almost all cereals marketed to children.

But do Americans really need health claims on food products? You might think that any relatively unprocessed food from a plant or animal ought to qualify as healthy without needing FDA approval, and you would be right. But health claims aren’t about health. They are meant to get people to buy food products, not real foods like fruit, vegetables, grains, nuts, meat, poultry, dairy, eggs, or fish.

Food companies love the term “healthy” because it gets people to buy food products.

 

The history of “healthy”

How did we get to where the FDA needs to require a product to contain real food to be considered “healthy”? Blame KIND bars.

In 2015, KIND (then a small private company, but now owned by Mars) advertised its bars as healthy because they contained whole foods like grains and nuts. But nuts have more fat than the FDA allowed at the time for products to be labeled as “healthy.” The FDA warned KIND that its bars violated the rules for health claims.

KIND fought back. It filed a citizens’ petition arguing that even though nuts are higher in fat than the FDA allowed, they are healthy. The FDA could hardly argue otherwise — of course nuts are healthy — and it backed off. It permitted KIND to use the term and said it would revisit its long-standing definition of “healthy.” That was good news for KIND.

At the time, the FDA’s definition of “healthy” set upper limits for fat, saturated fat, sodium, and cholesterol; required at least minimal amounts of one or more vitamins or minerals; and said nothing about sugars. So the new FDA proposals break new ground in simplifying the nutritional criteria and in putting a limit on sugars.

 

Front-of-package symbols

These, too, have a long history with the FDA. In the early 1990s, when the agency was writing the rules for Nutrition Facts labels on food products, it tested public understanding of several prototype designs. As it happened, nobody could understand any of the samples very well, so the FDA picked the one that was the least poorly understood. Soon afterward, food companies and health organizations developed symbols that would allow buyers to recognize at a glance which products were supposed to be good for them.

By 2010, more than 20 such symbols were on food packages. The FDA commissioned the Institute of Medicine to do studies of front-of-package labeling. The Institute’s first report on the subject examined the strengths and weaknesses of all of the symbols cluttering up the labels of processed foods, and recommended that the FDA develop a single symbol that would cover just calories, saturated fat, trans fat, and sodium. Why not sugars too? The Institute said calories took care of them.

But the Institute’s second report did include sugars. It recommended a front-of-package labeling system that would give food products zero, one, two, or three stars (or check marks) depending on how little they had of the undesirable nutrients.

This idea so alarmed food manufacturers that they quickly developed the Facts Up Front labeling system in use today.

This, in my view, is so obfuscating that nobody pays any attention to it. But this scheme, coupled with industry pushback, was all it took to get the FDA to drop the entire idea of a symbol that would tell people what not to eat.

Here we are a decade later with the FDA’s current proposal. This plan is strong enough to exclude huge swaths of supermarket products from self-identifying as “healthy.” Products bearing the “healthy” symbol will have to contain real food and be low in saturated fat, salt, and sugar, as called for by federal dietary guidelines.

The new rules won’t stop “healthy” products from being loaded with additives and artificial sweeteners. And the FDA won’t require warning labels for unhealthy products, which work better than other symbols. But these proposals are a marked improvement over the current situation.

And the FDA might do more. It could look into the idea of warning labels. It already promises to make a decision about the other ambiguous marketing term, “natural.” A decision on that one can’t come soon enough.

As for “healthy,” the FDA is seeking feedback on its proposals. Instructions for filing comments, which can be made until Dec. 28, 2022, are at Food Labeling: Nutrient Content Claims; Definition of Term “Healthy.

I can’t wait to see what companies wanting to sell ultra-processed food products as “healthy” will have to say about this.

Marion Nestle is professor emerita of nutrition, food studies, and public health at New York University, author of the Food Politics blog, and author of the new memoir, “Slow Cooked: An Unexpected Life in Food Politics” (University of California Press, October 2022).

***********

For 30% off, go to www.ucpress.edu/9780520384156.  Use code 21W2240 at checkout.

 

 

Jul 19 2022

The failing FDA: What is to be done?

Everyone is worried about the FDA (or should be) and I’ve been collecting suggestions for how to fix it.  I have three so far.

I.  Move food safety out of FDA and into a new Food Safety Administration. 

This would be housed (as FDA is) in the Department of Health and Human Services (HHS).

Senators Durbin, Blumenthal, and DeLauro have proposed legislation to do this.  The bill text is here and a fact sheet here.

  • “In recent years, FDA has been plagued by one failure after another—from a failure to properly recognize the dangers of prescription opioids, to a failure to protect children from e-cigarette products, to a failure to properly ensure the safety of our nation’s food supply,” said Durbin. “The sad reality is that FDA seems unwilling or unable to use their authority to protect Americans from preventable illness and death.
  • “Americans deserve to know the food on their plates is safe to eat,” said Blumenthal. “By protecting consumers from foodborne illnesses and acting swiftly to respond to recalls, the Food Safety Administration will improve the safety of our nation’s vital food supply.”
  • “Food safety is currently a second-class citizen at the Food and Drug Administration,” said DeLauro. “Right now, there are no food policy experts in charge of food safety at the FDA.”

II.  Move all food functions out of FDA into a separate agency.

This is proposed by several public action groups:  Consumer Reports, STOP Foodborne illness, the Environmental Working Group, and Healthy Babies Bright Futures.

[The] groups discussed the need for congressional action to separate the food portion of the Food and Drug Administration into a separate agency under the Depart of Health and Human Services. The agency would be solely devoted to the food side of the FDA, which oversees 80 percent of the nation’s food supply.

These groups have not developed specific details about how this might work.

III.  Move FDA’s food functions into USDA.

This proposal comes from Jerry Mande, former FDA and USDA official:  “A Farm to Fork approach to Fixing FDA’s food program.”

USDA is best positioned to succeed due to its history and mission. Created by President Abraham Lincoln to be the “people’s department,” USDA has the comprehensive resources and authorities needed to succeed. These include its 15 nutrition assistance programs and their $175 billion budget, its farm executive directors in every state and its transformative extension agents in literally every county, and the nation’s leading food and nutrition research programs.

Specifically, we propose that the FDA’s Center for Food Safety and Nutrition (CFSAN) merge with USDA’s Food and Nutrition Service (FNS) and Food Safety and Inspection Service (FSIS) under one Food, Nutrition and Health mission area at the USDA.

The Government Accountability Office has been calling for a separate food safety agency since at least 1990.  Its idea would be to combine the food safety functions of FDA (generally, plant foods and food products), USDA (generally, animal foods), and other federal agencies.  From a food safety perspective, that makes sense.

But what about FDA’s other food functions, such as oversight of  food ingredients, labels, and health claims?

And what about food advertising (FTC), health risks (CDC), etc?

What’s good about this is that doing something to strengthen food regulation is on the agenda.

How best to do it?

Ultimately, it’s up to Congress.

Jun 3 2020

Meat: the ongoing saga

If you want to understand why meat has become the focus of political fights about the effects of Covid-19, it helps to start with why the meat industry is so powerful.

I’ve always explained it this way: cattle are raised in every state, every state has two senators, every senator attracts hordes of lobbyists.

Food Safety News takes a deeper dive:

The meat industry effectively controls the Senate and House of Representatives by stopping a bill before it even reaches the floor. All legislation related to food and agriculture crosses the desks of the respective Agriculture Committees, so effort is targeted to build relationships, tailor strategic communications, and send influential campaign contributions to stay on the pulse of new developments.  For bills that do reach the floor, swift action is taken.

Over the years, proposals to have meat processors become partially or fully responsible for the cost of USDA inspections, which are currently provided without cost for routine operation, are quickly shot down as “unwise and unnecessary,” without explanation or discussion. Ironically, industry also seeks to reduce the presence of USDA inspectors by seducing the agency into allowing their workers to complete the tasks on their tab– but more on that later.

Yesterday’s Politico: has this headline “As meatpacking plants reopen, workers terrified of coronavirus risk” [this may be behind a paywall]

The latest Agriculture Department figures show that U.S. meat production is returning to nearly last year’s capacity, accomplishing the White House’s goal of keeping the food supply steady during the pandemic…At least 44 meatpacking workers have died from the virus and more than 3,000 have tested positive, according to the United Food and Commercial Workers Union. About 30 plants have closed in the past two months, affecting more than 45,000 workers.

A spokesperson for the Occupational Safety and Health Administration, the agency responsible for worker safety, told POLITICO that it has received more than 4,400 Covid-19-related safety complaints, but has issued only a single citation related to the pandemic….An employee at a JBS plant in Greeley, Colo., where eight workers have died from the virus, told POLITICO that although the company has required social distancing in break rooms and other areas, workers remain standing shoulder to shoulder on assembly lines. The employee was granted anonymity out of concern about retribution from the company after speaking out.

Some other items about the meat situation:

Dec 3 2019

The latest Romaine lettuce outbreak: Just say no.

The CDC continues to track the latest outbreak of illnesses caused by eating Romaine lettuce contaminated with E. coli O157:H7.

The outbreak at a glance:

The FDA’s advice:

Consumers should not eat romaine lettuce harvested from Salinas, California. Additionally, consumers should not eat products identified in the recall announced by the USDA on November 21, 2019.

A former FDA official, Stephen Ostroff, says:

With five multistate outbreaks in less than two years, it’s clear there’s a serious continuing problem with E. coli O157:H7 and romaine lettuce. The natural reservoir for this pathogen is ruminant animals, especially cattle. Moreover, one particular strain of E. coli seems to have found a home in the growing regions of central coastal California, returning each fall near the end of the growing season.

It’s not clear where this strain is hiding. Cattle? Water sources? Elsewhere? What is clear is that additional steps must be taken to make romaine safer.

The New Food Economy emphasizes some particularly distressing aspects of this particular outbreak.

  • It is caused by the same strain of E. coli O157:H7 that caused outbreaks linked to leafy greens in 2017 and to Romaine lettuce in 2018.
  • This strain of E. coli seems particularly virulent: 39 of the 67 cases had to be hospitalized.
  • The source has not yet been traced.

Consumer Report’s advice: ”

People should avoid all romaine lettuce and that any currently in refrigerators should immediately be thrown out because of the risk of E. coli contamination…CR’s experts think it is prudent and less confusing for consumers to avoid romaine altogether, especially because romaine is also sold unpackaged and in restaurants, and customers can’t always be sure of the origin that lettuce.  “Much of the romaine lettuce on the market at this time of year is from Salinas,” says James E. Rogers, Ph.D., director of food safety research and testing at Consumer Reports.

Food safety lawyer Bill Marler says enough is enough; It’s time to put warning labels on Romaine lettuce.

Marler’s advice: when in doubt, throw it out.

My comment:  Contamination of vegetables with toxic E. coli means that the vegetables somehow came in contact with waste from farm animals or wild animals or birds.  The most likely suspect is Confined Animal Feeding Operations (CAFOs) or large dairies because they produce so much animal waste.  If one animal is infected under crowded CAFO conditions, other animals also will be infected (but cows don’t show symptoms).

Preventing lettuce contamination means that CAFOs must manage their waste so that it is not infectious (USDA and EPA regulated) and vegetable farms must keep infected water from contaminating their crops (FDA regulated).  All of this means following food safety procedures to the letter, but also in spirit.

Constant Romaine outbreaks are further evidence for the need for consistency in USDA and FDA food safety policies, and a reminder that calls for a single, united food safety agency have been coming for more than 40 years.  Surely, it’s time.

Jun 25 2018

Trump’s government reorganization plan: really?

The Trump Administration announced its new plan to reorganize government.  Obviously, this affects the agencies dealing with agriculture, food, and nutrition issues—USDA, FDA, and FDA’s parent agency, HHS.  Here is my translation of the major shifts being proposed:

  • Move most of USDA’s nutrition programs—SNAP, WIC, the Child and Adult Care Food Program, and the Farmers’ Market Nutrition Program—to HHS.
  • Move FDA’s food safety oversight to USDA, putting USDA in charge of all food safety.
  • Downsize the Public Health Service Commissioned Corps.

Congress would have to vote on all this so there’s no point in going too deeply into the weeds at this point, but I have just a few comments:

  • Putting all food safety oversight in one agency is a good idea, but not if it’s USDA.  USDA’s principal purpose to to support agribusiness.  Holding agribusiness responsible for food safety puts USDA in conflict of interest.
  • Moving SNAP and WIC into HHS (or whatever its new name will be) would make sense if HHS weren’t already overwhelmed by everything else it has to deal with (more than a trillion dollars in spending).
  • The proposal still leaves school breakfasts and lunches and commodity programs in USDA, meaning that food assistance programs will still be split between USDA and HHS.
  • Downsizing the Commissioned Corps doesn’t make much sense either.  Public health needs all the health it can get.

Whatever happens with this is unlikely to happen quickly.  USDA will not be happy about losing SNAP’s $80 billion a year or WIC’s $6 billion budget.

Many other agencies are also affected by these proposals.  My prediction: Congress will have a lot of trouble coming to agreement on these ideas.

Maybe this is just another attempt to distract us from more pressing matters.

Law Professor Timothy Lytton, an expert on food regulatory policy, has plenty to say about why moving food safety to USDA won’t work (in my paraphrasing):

  • Congressional committees are unlikely to support any reorganization that would reduce their power.
  • Industry associations are unlikely to support a reorganization that would disrupt their influence with existing agencies.
  • The two agencies are different in jurisdiction, powers and expertise; a merger would require a complete overhaul of federal food safety laws and regulations, a task of extraordinary legal and political complexity.
  • A merger might create new forms of fragmentation.
  • Reorganization is expensive and will take years.  The payoff is unclear.

As I’ve explained before, plans for a single food safety agency have been in the works for years, but have encountered many barriers.  The Food Safety Modernization Act was meant to be step #1 in a three-step process:

  1. Pass and implement rules governing FDA’s oversight of pretty much all foods except meat and poultry (this is now done).
  2. Fix USDA’s food safety rules governing meat and poultry so they are consistent with FDA’s (in the talking stage, hopefully).
  3. Merge the food safety responsibilities in one agency.

These proposals, alas, ignore step #2.  Good luck with that.