by Marion Nestle

Search results: single food agency

Jul 21 2008

GAO looks at international food safety

The Government Accountability Office, long a proponent of overhauling the U.S. food safety system and putting it under the aegis of a single food safety agency, has produced more evidence for its view (I love this title): Food Safety: Selected Countries’ Systems Can Offer Insights into Ensuring Import Safety and Responding to Foodborne Illness. The countries they looked at have farm-to-table safety systems in place, place primary responsibility on food producers (what a concept!), deal with risk intelligently, and have mandatory recall authority. We could do this too, maybe?

May 27 2008

Food safety politics again

Here’s a useful post from Science Progress (in which I am quoted) on the push to fix the U.S. food safety system by creating a single food safety agency. It comes with an instructive diagram of the various agencies now involved–this alone is a good reason why the system needs a fix.  Science Progress is a project of the Center for American Progress, of which I had not heard until now.

Nov 22 2023

An update on sugar (just in time for Thanksgiving)

While producers of sugar cane celebrated National Real Sugar Day on October 14, the New York City Council voted to require chain restaurants to post warning labels on sodas and other menu items that exceed to-be-defined limits on added sugars.

Mayor Eric Adams signed the Sweet Truth Act, which gives the city until 2024 to set standards and design the icon, and gives chain restaurants until 2025 to comply.

Meals at fast food and fast casual restaurants can be exceedingly high in added sugars, amounts that far exceed the FDA’s daily recommendation for consumption of 50 grams per day. Even most “small” fountain sodas sold at leading fast food chains contain more than a day’s worth of added sugars. Added sugars have been linked to weight gain in children and adults. Sugary drinks may also contribute to type 2 diabetes and heart disease.

In a video, New York City Health Commissioner, Dr. Ashwin Vasan, explains why sugar redction is a good idea.

Where is the FDA in all this?  It held a public meeting on the need for sugar reduction.  What it will do as a result remains to be seen, but the New York City action is surely a nudge.

In the meantime, the Government Accountability Office has some things to say about the U.S. Sugar Program.  It sums up the issues concisely.

The Department of Agriculture administers the U.S. sugar program to support domestic sugar production through tools such as limiting the supply of sugar.

The program creates higher sugar prices, which cost consumers more than producers benefit, at an annual cost to the economy of around $1 billion per year.

The program also restricts the amount of sugar entering the U.S. at a low tariff. The tariff restrictions are applied using a method based on 40-year-old data that doesn’t reflect current market conditions. This has led to fewer sugar imports than expected.

We recommended that USDA evaluate its method for restricting imports.

Comment: Here is a situation in which policies for sugar production and import intersect with policies for sugar and health in peculiar ways.  The objective of import policies is to restrict them in order to keep prices higher as a means to protect domestic sugar producers.

Ordinarily, food policies are designed to keep prices low—but not in this case (chalk this up to effective lobbying by cane and beet sugar producers, and the power of lobbyists in sugar-producing states).

Also ordinarily, higher prices would reduce demand, but sugar prices are nowhere near high enough to influence demand, which is one reason why this system continues.

Current policies are estimated to cost the public as much as $3.5 billion a year; divided by 350 million Americans means that the policies cost you an extra $10 per year for the sugar you buy—nowhere near enough to affect consumption.

Disparate goals for sugar are yet another reason why a single food agency overseeing the entire food system would be useful for reconciling these kinds of problems.

Sep 29 2011

Since when did cantaloupe become a WMD*?

Are you as puzzled about the latest cantaloupe outbreak as I am?  This time it’s Listeria again (see previous post on this particular pathogen).

According to the CDC, 72 people have been infected with the strains of Listeria associated with the outbreak in 18 states.  Most appalling,  13 people have died.

The CDC says that the people who have become ill range from 35 to 96 years, with a median age of 78 years.  Most are over age 60 or have health conditions that weaken the immune system.  Pregnant women are at especially high risk as are their fetuses.

As always, the recall occurred after most of the cases were reported to the CDC.  The cantaloupe were traced to Jensen Farms, which issued a recall on September 14.

Why cantaloupe?  They are, after all, grown in dirt and their skin is rough, textured, and has plenty of places for bacteria to hide.  People pick up Listeria by handling the fruit and cutting into it.  FDA’s information page lists the recalls and press releases on the Jenson Farms outbreak.

The FDA’s advice: throw it out.

Do not try to wash the harmful bacteria off the cantaloupe as contamination may be both on the inside and outside of the cantaloupe. Cutting, slicing and dicing may also transfer harmful bacteria from the fruit’s surface to the fruit’s flesh.

What do food safety experts say you have to go through to avoid getting sick from eating cantaloupe?

  • Wash the melon under running water with a clean vegetable brush.
  • Blot with paper towels to remove excess water.
  • Put melon on a clean surface, one that hasn’t come into contact with meat or poultry or other foods that could cause cross-contamination.
  • Cut off the stem end about 3/4 to 1 inch from the end, using a clean kitchen knife.
  • Place melon on a clean cutting board, plate, or other clean surface with the cut end facing down.
  • Using a clean knife, cut the melon from the blossom end to the stem end.
  • Follow this by washing the knife with clean running water and setting it aside.
  • Gently scrape out the seeds with a clean spoon and cut the melon into slices or whatever is desired.
  • Don’t use dish soap or detergent; cantaloupes can absorb detergent residues.
  • Do not allow the rind to touch any part of the edible fruit.
  • Melon that isn’t eaten should be peeled, covered and refrigerated.
  • Discard any melon that has been at room temperature for longer than 2 hours, or 1 hour when the temperatures are over 90 degrees F.
  • Follow these procedures for all melons, no matter where they were grown.

What?  No HazMat suit?

We are talking about cantaloupes here.

How about a food safety system where everyone makes sure—and tests—that Listeria don’t get on cantaloupe in the first place.

Single food agency anyone?

_____

*Translation: Weapon of Mass Destruction

Jul 7 2009

Michael Taylor appointed to FDA: A good choice!

On Monday this week, Michael Taylor began his new job as special assistant to the FDA Commissioner for food safety.  He will be in charge of implementing whatever food safety laws Congress finally decides to pass.

I know that what I am about to say will surprise, if not shock, many of you, but I think he’s an excellent choice for this job. Yes, I know he worked for Monsanto, not only once (indirectly) but twice (directly). And yes, he’s the first person whose name is mentioned when anyone talks about the “revolving door” between the food industry and government. And yes, he signed off on the FDA’s consumer-unfriendly policies on labeling genetically modified foods.

But before you decide that I must have drunk the Kool Aid on this one, hear me out.  He really is a good choice for this job.  Why?  Because he managed to get USDA to institute HACCP (science-based food safety regulations) for meat and poultry against the full opposition of the meat industry — a truly heroic accomplishment.  His position on food safety has been strong and consistent for years.  He favors a single food agency, HACCP for all foods, and accountability and enforcement.  We need this for FDA-regulated foods (we also need enforcement for USDA-regulated foods, but he won’t be able to touch that unless Congress says so).  So he’s the person most likely to be able to get decent regulations in place and get them enforced.

I say this in full knowledge of his history.  In the 1990s, Mr. Taylor held positions in both FDA and USDA and his career in these agencies is complicated.  As I explained in my 2003 book, Safe Food  (see the endnotes for full documentation), Mr. Taylor began his career as a lawyer with the FDA. When he left the FDA, he went to work for King & Spalding, a law firm that represented Monsanto, the company that developed genetically engineered bovine growth hormone (BGH), corn, and soybeans.

He revolved back to the FDA in 1991 as deputy commissioner for policy, and he held that position during the time the agency approved Monsanto’s BGH. At the time of the review, he had been with FDA for more than two years. This made him exempt from newly passed conflict-of-interest guidelines that applied only to the first year of federal employment.  He also was a coauthor of the FDA’s 1992 policy statement on genetically engineered plant foods, and he signed the Federal Register notice stating that milk from cows treated with BGH did not have to be labeled as such.

For whatever it is worth, a 1999 lawsuit and GAO report revealed considerable disagreement about these decisions within FDA. These also revealed that Mr. Taylor had recused himself from matters related to Monsanto’s BGH and had “never sought to influence the thrust or content” of the agency’s policies on Monsanto’s products.  I can’t tell whether there were ethical breaches here or not, but there is little question that his work at FDA gave the appearance of conflict of interest, if nothing more.

But wait! Watch what happened when he moved to USDA in 1994 as head of its Food Safety and Inspection Service (FSIS). Just six weeks after taking the job, Mr. Taylor gave his first public speech to an annual convention of the American Meat Institute. There, he announced that USDA would now be driven by public health goals as much or more than by productivity concerns. The USDA would soon require science-based HACCP systems in every meat and poultry plant, would be testing raw ground beef, and would require contaminated meat to be destroyed or reprocessed. And because E. coli O157.H7 is infectious at very low doses, the USDA would consider any level of contamination of ground beef with these bacteria to be unsafe, adulterated, and subject to enforcement action.  Whew.  This took real courage.

The amazing thing is that he actually made this work.  Now, HACCP rules apply more to USDA-regulated products than to FDA-regulated products. This new appointment gives Mr. Taylor the chance to bring FDA’s policies in line with USDA’s and even more, to make sure they are monitored and enforced.

In Safe Food, I summarize Mr. Taylor’s position on food safety regulation from 2002. Then, he argued for, among other things:

  • A single agency accountable for providing consistent and coordinated oversight of food safety, from farm to table.
  • Institution of Pathogen Reduction: HACCP, with performance standards verified by pathogen testing, at every step of food production.
  • Recall authority, access to records, and penalties for lapses in safety procedures.
  • Standards for imported foods equivalent to those for domestic foods.
  • Food safety to take precedence over commercial considerations in trade disputes.

Yes, he revolved back to Monsanto after leaving FDA but he didn’t stay long. He left Monsanto for Resources for the Future, a think tank on policy issues.   In 2007, he went to academia and joined the food policy think tank (see his bio) at George Washington University.  There, he produced the excellent food safety report I mentioned in a previous post, which repeats these points. This is about as good a position on food safety as can be expected of any federal official.

I wish him all the luck in the world in getting the safety of FDA-regulated foods under control. For those of you who are still dubious, how about giving him a chance to show what he can do?  But do keep the pressure on – hold his feet to the fire – so he knows he has plenty of support for doing the right thing.

[Posted from Skagway, Alaska, en route to Fairbanks]

Jun 30 2008

The tomato (maybe?) saga continues

The epidemic of illness caused by the unusual saintpaul type of Salmonella has now affected more than 800 people, and federal agencies seem more than perplexed about its source. The FDA says tomatoes, and called for their removal from the market, an action with devastating consequences for the tomato industry. But cases are still turning up. Perhaps that is why the CDC thinks maybe something else might be the cause. Salsa? Guacamole? The produce industry is understandably interested and two websites are excellent sources of day-to-day information: the straight-news Packer, and the tell-it-like-it-is Perishable Pundit. Go to the FDA website for updates on the ongoing investigation and also provides lists of tomatoes safe to eat. Part of the difficulty in following this story is that two federal agencies are involved: the FDA and the CDC. The CDC has its own version of events (with useful maps of where the cases are in the U.S.). The USDA , which only deals with animal foods, doesn’t seem to be part of this one. It should be. The ultimate source of this outbreak has to be animal waste. This tomato (?) outbreak is precisely why we need a single food agency to oversee food safety. When, oh when?

Update, July 1: The Wall Street Journal reviews the outbreak and explains why the produce and restaurant industries are so angry.

Update, July 2: The Wall Street Journal quotes the Secretary of Health and Human Services, Mike Leavitt , saying that because multiple countries and multiple agencies are involved in the investigation, “it shows the need for better cooperation.” No. It shows the need for a single food agency!

Update, July 3: I’ve just discovered USA Today’s nifty time line of the tomato saga.

Jan 14 2026

The MAHA Dietary Guidelines V. The Alcohol Non-Recommendation

The Dietary Guidelines for America 2025-2030 simply say “Limit alcoholic beverages: Consume less alcohol for better
overall health.”  They go on to specify who should not drink alcohol.

People who should completely avoid alcohol include pregnant women, people who are recovering from alcohol use disorder or are unable to control the amount they drink, and people taking medications or with medical conditions that can interact with alcohol. For those with a family history of alcoholism, be mindful of alcohol consumption and associated addictive behaviors.

This guideline

  • Does not specify what is meat by “limit” or “less.”
  • Does not mention cancer as a risk of alcohol consumption.

These are big issues.  Excessive alcohol intake poses problems for society as well as for individuals: car accidents and gun violence, for example.

From a public health perspective, the lower the overall level of alcohol consumption in a population, the fewer the health and societal problems it causes.  The overall message always should be: drink as little alcohol as possible.

This message is complicated by evidence, highly contested, that low levels of alcohol might reduce risks for heart disease and overall mortality.  Even if correct, advice about alcohol would need to balance the purported benefits for heart disease against risks for cancer, particularly breast cancer.

The Biden-era 2025 Dietary Guidelines Advisory Committee did not discuss alcohol because the agencies were waiting for the results of commissioned reports on alcohol and health.  As it happened, three reports came out just after the DGAC submitted its report late in 2025.

Even so, the take-home lesson from all of these reports is that less alcohol is better.

At issue is how much less.

As I’ve explained previously, the dietary guidelines have long stated that 2 drinks a day for men and 1 for women (because women metabolize alcohol differently) is a safe amount.

The omission of these limits is difficult to interpret.  Do these guidelines consider those limits too low or too high?

At the press conference, Mehmet Oz said:

Alcohol is a social lubricant that brings people together. In the best-case scenario, I don’t think you should drink alcohol, but it does allow people an excuse to bond and socialize, and there’s probably nothing healthier than having a good time with friends in a safe way..You look at the Blue Zones, for example, around the world, where people live the longest. Alcohol is sometimes part of their diet…Again, small amounts. There is alcohol on these dietary guidelines, but the implication is don’t have it for breakfast.

Yes, but what is a “small amount?”  And what about cancer risk?  Shouldn’t people be warned?

As Roni Rabin put it:

Though there is robust debate within the medical community as to the relationship between moderate drinking and various forms of cardiovascular disease, there is more scientific certainty about the link between alcohol and at least seven types of cancer. Warnings about alcohol increasing the risk of breast cancer were included in the dietary guidelines 25 years ago. Former Surgeon General Dr. Vivek Murthy last year called for putting cancer warning labels on alcoholic beverages, similar to those for cigarettes.

The alcohol industry works unceasingly to convince everyone that alcohol poses no health risks.  Unfortunately, it does.

Yes, consume less, but how much less?  The guidelines leave this up to you to decide.

I see these dietary guidelines as a big win for the alcohol industry.

No wonder it supports them so enthusiastically: Distilled Spirits, Beer & Wine Associations Support New Health and Human Services 2025-2030 ‘Dietary Guidelines for Americans’

Moderation?  Whatever you think it means.

Dec 16 2025

USDA’s Regenerative Farming Initiative: Real or Greenwashing?

Regenerative is the new buzzword for sustainable agricultural practices.  Unfortunately, the term is undefined.

I like the approach of the Real Organic Project: regenerative begins with—and extends—certified organic production methods.

The USDA has now adopted the term for its own purposes: USDA Launches New Regenerative Pilot Program to Lower Farmer Production Costs and Advance MAHA Agenda.  It

announced a $700 million Regenerative Pilot Program to help American farmers adopt practices that improve soil health, enhance water quality, and boost long-term productivity, all while strengthening America’s food and fiber supply…(HHS) is also investing in research on the connection between regenerative agriculture and public health, as well as developing public health messaging explaining this connection.

This sounds great, but what does it mean?  Cutting through the rhetoric,

In FY2026, the Regenerative Pilot Program will focus on whole-farm planning that addresses every major resource concern—soil, water, and natural vitality—under a single conservation framework. USDA is dedicating $400 million through the Environmental Quality Incentives Program (EQIP) and $300 million through the Conservation Stewardship Program (CSP) to fund this first year of regenerative agriculture projects.

Oh.  It’s investing in two existing programs that already paid farmers to reduce tilling, plant cover crops, and manage manure.

As Marcia Brown explains in Politico

It’s the most significant commitment toward regenerative agriculture the Trump administration has announced yet, but it comes months after it axed similar Biden-era conservation programs and as it pushes ahead with approvals for new pesticides that are considered forever chemicals.

She quotes Stephanie Feldstein of the Center for Biological Diversity:

Regenerative agriculture needs to be more than just buzzwords Big Ag uses to greenwash business as usual…While the Trump administration promises money for sustainable practices, it continues to cut conservation staff, support the pesticide industry, roll back environmental laws and play trade war games that hurt farmers and our food system.

Comment

All USDA agricultural support programs should require farmers to produce foods in ways that minimize damage to the environment.  This initiative needs to come with specific requirements, clear definitions, and accountability.  These are tiny programs in the context of USDA’s $20 billion annual expenditure on farm supports.  If the agency is serious about producing food more sustainably—which it absolutely should be—it will define what it means by regenerative and apply those principles to all its programs.

Otherwise, this is flat-out greenwashing.