by Marion Nestle

Search results: app

Jan 16 2013

Coca-Cola fights obesity? Oh, please.

In case you missed all the publicity about Coca-Cola’s new ad campaign positioning the company as a force for public health, take a look at its new two-minute TV ad.

The video—how much do these things cost?—argues that the company is producing lower-calorie products in smaller sizes and promoting community activity, that all calories count, and that it’s up to you to fit Coke into your healthy active lifestyle.

The ad is an astonishing act of chutzpah, explainable only as an act of desperation to do something about the company’s declining sales in the U.S. and elsewhere.

If Coke really wanted to help prevent obesity, it would STOP:

  • Targeting its “drink more Coke” marketing to kids.
  • Targeting marketing to low-income minorities.
  • Lobbying and spending a fortune to defeat soda taxes and caps on soda sizes.
  • Fighting attempts to remove vending machines from schools.
  • Pricing drinks so the largest sizes are the best value.
  • “Bribing” health professions organizations to shut up about research linking sugar-sweetened beverages to poor diets and weight gain.
  • Pushing Coke sales in developing countries where rates of obesity and related conditions are skyrocketing.

Instead, it’s doing all these things, but not talking about them in videos.

The company is supposed to be releasing a second video tonight, explaining how to work off the “140 happy calories” in a soda by dog-walking, dancing, or laughing. If only.

I can’t wait.

Addition, January 18:  Someone who calls himself John Pemberton has gone to the trouble of presenting the 2-minute commercial with a somewhat different narrative—the real story about Coca-Cola and obesity.  If that link doesn’t work, try this one.

Jan 14 2013

FDA issues food safety rules–at long last

I’m catching up with events that occurred while I was out of the country.  One was the release by FDA of two of its long-awaited proposals for food safety rules.

These go into the Federal Register on January 16. But they were announced on January 4, perhaps to commemorate the two-year anniversary of President Obama’s signing the Food Safety Modernization Act authorizing these rules.

The two massive sets of proposed rules, 680 and 547 pages, respectively, are:

Still to come: proposed rules for

  • Food importers
  • Preventive controls for animal feed
  • Accreditation of third-party auditors

Notice that all of these are proposals.  Terrific as it is to have them released, no breath-holding is in order.

Once the proposals appear in the Federal Register, interested parties will have 120 days to comment.  It will probably take a year for the FDA to write final rules.   For the produce standards at least, larger farms get 2 years before implementation kicks in.  Smaller farms get 3 or 4 more years to figure out how to comply.

Some farms, such as those bringing in less than $500,000 per year, are exempt.  Chalk that up to successful lobbying by small farmers.

The FDA estimates that the new rules will cost large farms about $30,000 a year, and small farms $13,000.   It says that following the rules will prevent 1.75 million cases of foodborne illness a year and save more than $1 billion in costs.

The rules for produce focus on prevention of contamination through:

  • Agricultural water
  • Biological soil amendments
  • Poor worker hygiene
  • Domesticated and wild animals
  • Equipment, tools and buildings.

All food producers will need to develop, submit, and follow a written food safety plan that includes:

  •  A hazard analysis
  • Preventive controls
  • Monitoring procedures
  • Corrective action procedures
  • Verification procedures
  • A recall plan

That’s the basic outline.  The devil is in the details and in this case there are plenty of them (I have much sympathy for whoever has to write these things).  The proposals devote hundreds of pages to definitions.  Here, for example, is FDA’s summary of its definition of farm and farm activities.  Hint: RAC = Raw Agricultural Commodity.

  • The basic purpose of farms is to produce RACs and RACs are the essential products of farms.
  • Activities that involve RACs and that farms traditionally do for the purposes of growing their own RACs, removing them from the growing areas, and preparing them for use as a food RAC, and for packing, holding and transporting them, should all be within the definition of “farm” in §§ 1.227 and 1.328.
  • Activities should be classified based in part on whether the food operated on is a RAC or a processed food, and on whether the activity transforms a RAC into a processed food.
  • Activities farms may perform on others’ RACs should appropriately be classified as   manufacturing/processing, packing, or holding in the same manner as these activities are classified off-farm when the RACs are to be distributed into commerce.
  • Manufacturing/processing, packing, or holding food– whether RACs or processed foods, from any source–for consumption on the farm should remain within the farm definition.

I include this example to illustrate what food producers are up against.  It explains why practically every group commenting on the proposals said the same things: “we are glad they are out but must reserve comment until we—and our lawyers—have a chance to go over the rules in detail.”

My guess is that we will be hearing plenty more about these reactions when they do.

In the meantime, the elephant in the room issue is funding.  The FDA’s budget is already overstressed.  How can it possibly add monitoring and enforcement responsibilities without additional staff and funding?  How can it get new resources from this Congress?

Recall: the FDA gets its funding from congressional agriculture appropriations committees, not health committees.

The FDA addresses the funding issue in a website Q and A:

G.5.  Does FDA have sufficient funding to implement the new rule?  The funding we have available through the annual budget cycle and fees impacts the number of FTEs we have and will be a factor in the way that FDA handles its significant and far-ranging activities, including the way that this legislation is implemented… Without additional funding, FDA will be challenged in implementing the legislation fully without compromising other key functions. We look forward to working with Congress and our partners to ensure that FDA is funded sufficiently to achieve our food safety and food defense goals.

Indeed.

To submit a comment:

  • Go to http://www.regulations.gov.
  • Refer to Docket No. FDA-2011-N-0920.
  • Do it by May 16.
Jan 11 2013

The Leanwashing Index: Yes!

I was unfamiliar with the Leanwashing Index, but am delighted to learn about it.  EnviroMedia launched it in 2012 to discourage advertisers from using absurdities to push products.

EnviroMedia explains the inspiration for the Index: the appearance of the word “Superfood” on Lake Superior State University’s 38th annual List of Words to be Banished.

Here’s the 2013 Leanwashing list:

  • Natural
  • Made With
  • Whole Grains
  • Light
  • 100 Calorie

Away with all of them!  (I can think of plenty more.  Send your suggestions to the site.)

Here’s a prime example:

And while we are on the subject of whole grains, you might want to take a look at Colbert’s latest “Thought for Food.”

Enjoy the weekend!

Jan 10 2013

Predictions for 2013 in food politics

For my monthly (first Sunday) Food Matters column in the San Francisco Chronicle, I devote the one in January every year to predictions.  Last year I got them all pretty much on target.  It didn’t take much genius to figure out that election-year politics would bring things to a standstill.  This year’s column was much harder to do, not least because the FDA was releasing blocked initiatives right up to the printing deadline.

 Q: I just looked at your 2012 crystal ball column. Your predictions were spot on. But what about 2013? Any possibility for good news in food politics?

A: Food issues are invariably controversial and anyone could see that nothing would get done about them during an election year. With the election over, the big question is whether and when the stalled actions will be released.

The Food and Drug Administration has already unblocked one pending decision. In December, it released the draft environmental assessment on genetically modified salmon – dated May 4, 2012. Here comes my first prediction:

The FDA will approve production of genetically modified salmon: Because these salmon are raised in Canada and Panama with safeguards against escape, the FDA finds they have no environmental impact on the United States. The decision is now open for public comment. Unless responses force the FDA to seek further delays, expect to see genetically modified salmon in production by the end of the year.

Pressures to label genetically modified foods will increase: If approval of the genetically modified salmon does nothing else, it will intensify efforts to push states and the FDA to require GM labeling.

Whatever Congress does with the farm bill will reflect no fundamental change in policy: Unwilling to stand up to Southern farm lobbies, Congress extended the worst parts of the 2008 farm bill until September. Don’t count on this Congress to do what’s most needed in 2013: restructure agricultural policy to promote health and sustainability.

The FDA will start the formal rule-making process for more effective food safety regulations: President Obama signed the Food Safety Modernization Act in January 2011. Two years later, despite the FDA’s best efforts, its regulations – held up by the White House – have just been released for public comment. Lives are at stake on this one.

The FDA will issue rules for menu labels: The Affordable Care Act of 2010 required calorie information to be posted by fast-food and chain restaurants and vending machines. The FDA’s draft applied to foods served by movie theaters, lunch wagons, bowling alleys, trains and airlines, but lobbying led the FDA to propose rules that no longer covered those venues. Will its final rules at least apply to movie theaters? Fingers crossed.

The U.S. Department of Agriculture will delay issuing nutrition standards for competitive foods: When the USDA issued nutrition standards for school meals in January 2012, the rules elicited unexpected levels of opposition. Congress intervened and forced the tomato sauce on pizza to count as a vegetable serving. The USDA, reeling, agreed to give schools greater flexibility. Still to come are nutrition standards for snacks and sodas sold in competition with school meals. Unhappy prediction: an uproar from food companies defending their “right” to sell junk foods to kids in schools and more congressional micromanagement.

The FDA will delay revising food labels: Late in 2009, the FDA began research on the understanding of food labels and listed more relevant labels as a goal in its strategic plan for 2012-16. Although the Institute of Medicine produced two reports on how to deal with front-of-package labeling and advised the FDA to allow only four items – calories, saturated and trans fat, sodium and sugars – in such labels, food companies jumped the gun. They started using Facts Up Front labels that include “good” nutrients as well as “bad.”

Will the FDA insist on labels that actually help consumers make better choices? Will it require added sugars to be listed, define “natural” or clarify rules for whole-grain claims? I’m not holding my breath.

Supplemental Nutrition Assistance Program participation will increase, but so will pressure to cut benefits: Demands on Snap – food stamps – reached record levels in 2012 and show no sign of decline. Antihunger advocates will be working hard to retain the program’s benefits, while antiobesity advocates work to transform the benefits to promote purchases of healthier foods. My dream: The groups will join forces to do both.

Sugar-sweetened beverages will continue to be the flash point for efforts to counter childhood obesity: The defeat of soda tax initiatives in Richmond and El Monte (Los Angeles County) will inspire other communities to try their own versions of soda tax and size-cap initiatives. As research increasingly links sugary drinks to poor diets and health, soda companies will find it difficult to oppose such initiatives.

Grassroots efforts will have greater impact: Because so little progress can be expected from government these days, I’m predicting bigger and noisier grassroots efforts to create systems of food production and consumption that are healthier for people and the planet. Much work needs to be done. This is the year to do it.

And a personal note: In 2013, I’m looking forward to publication of the 10th anniversary edition of “Food Politics” and, in September, my new editorial cartoon book with Rodale Press: “Eat, Drink, Vote: An Illustrated Guide to Food Politics.”

Jan 8 2013

A Man. A Plan. Panamá!

On vacation in Panamá, I found few visible signs of food politics.

I had asked to visit the mountain site where genetically modified salmon are being raised in the mountains (see previous post).  Not a chance.

This made me even more curious.  I conducted an informal survey of every educated Panamanian I met:

  • Are you aware that genetically modified salmon are being raised in your country?
  • Do you care?

The answers: No and No.

I found only two exceptions: (1) a government official impressed by what he told me were five levels of security to make sure the fish don’t escape, and (2) an associate of the soon-to-open biodiversity museum (designed by Frank Gehry) who hoped that the museum could be a forum for such issues.

Both confirmed that the newspapers said nothing about GM salmon and that few people knew about them.

A chef’s reaction: Panamanian salmon!  He couldn’t wait to get some.

But I did see this Christmas display along the Avenida Balboa.

The Coca-Cola banner also says Alcaldía de Panamá: trabajando para ti (Mayor of Panamá City: working for you).

Happy new year!  Happy to be back.

Dec 28 2012

The FTC’s latest report on food marketing to kids: glass half full or empty?

Last Friday was a big day for releasing reports that federal agencies would rather keep quiet.  As I discussed in my previous post, the FDA released its long overdue environmental impact report on GM Salmon.

Today, let’s take a look at the FTC’s latest report on the state of food and beverage marketing aimed at children. This is a follow-up to the report the FTC issued in 2008.

The new report cites progress.  From 2006 to 2009, its press release says:

  • Total spending on food marketing to youth ages 2-17 dropped from $2.1 billion to $1.79 billion, mainly because of less spending on television advertising.
  • But spending on new media, such as online, mobile, and viral marketing, increased by 50 percent.
  • Cross-promotions that link marketed foods with popular children’s movies and TV characters increased from 80 children’s movies and TV shows to 120.
  • Cereals had 0.9 gram less sugar and 1.6 grams more whole grain.
  • Fast food was a  little lower in calories, sodium, sugar, and saturated fat.

The report concludes:

Despite the commendable progress, this report identifies areas where further efforts could be made by the food and beverage industry and the media industry to improve the nutritional quality of foods marketed to youth.

Whether you see this as good news or not such good news depends on whether you see the glass as half full or half empty.

If you are a half-full type, you will rejoice that food companies are voluntarily improving the nutritional quality of their products even if the improvements are small.

If you are a half-empty type (which, in this case, I am), you will be dismayed at the lack of real progress in reducing the marketing of junk foods to kids.

Companies must sell more and more products to grow their businesses.  They are under pressure to reduce such marketing and to improve the quality of the products they sell.  Neither change is likely to increase sales.   Hence: resistance to change.

As Andy Bellatti points out, small nutritional improvements are unlikely to have much of an effect on health: reducing the sugars by 0.9 grams can be interpreted as “better for you” but does not necessarily make a product a good choice.

And as Michele Simon’s interview with former marketer Bruce Bradley suggests, the data on which the FTC based its positive assessments may well have been gamed by the companies reporting it.

As I read this report, it provides plenty of evidence that stopping food and beverage marketing to kids is the issue that matters most to doing something to reverse childhood obesity.

The election is over.    Maybe Let’s Move! can revisit the marketing-to-kids issue.  Someone needs to do it.  And soon.

 

Dec 26 2012

The hazards of GM foods: patent protection and international relations

Writing in Slate, Fred Kaufman takes a fresh look at the controversies over genetically modified (GM) foods.  Forget the other issues, he says.   Pay attention to patents:

GM foods’ effect on health is uncertain, but their effect on farmers, scientists, and the marketplace is clear. Some GM foods may be healthy, others not; every genetic modification is different. But every GM food becomes dangerous—not to health, but to society—when it can be patented. Right now, the driving force behind the development of new genetic crop modifications is the fact that they possess the potential to be enormously profitable….

That brings me to the GM salmon, in particular AquAdvantage brand engineered to grow faster and bigger than wild salmon.

Last Friday (always a good time to release something controversial), the FDA let loose its draft environmental assessment on the GM salmon.  The draft finding of “no effect” is now open for comment.

I find the draft statement remarkable for two reasons.

  • It is dated May 4, 2012, suggesting that it was considered too political to release before the election.
  • It applies only to production of GM salmon outside the United States.

The FDA had already ruled that the salmon are safe to eat:

With respect to food safety, FDA has concluded that food from AquAdvantage Salmon is as safe as food from conventional Atlantic salmon, and that there is a reasonable certainty of no harm from consumption of food from triploid AquAdvantage Salmon. Further, FDA has concluded that no significant food safety hazards or risks have been identified with respect to the phenotype of the AquAdvantage Salmon.

With respect to environmental impact, the FDA says:

FDA preliminarily concludes that the development, production, and grow-out of AquAdvantage Salmon under the conditions proposed in the materials submitted by the sponsor in support of an NADA [New Animal Drug Application], and as described in this draft EA [Environmental Assessment], will not result in significant effects on the quality of the human environment in the United States.

AquAdvantage is not intended to be grown in the United States.  It is being raised on Prince Edward Island in Canada and in Panama and will be processed in Panama.

Under the proposed action, AquAdvantage Salmon would not be produced or grown in the United States, or in net pens or cages, and no live fish would be imported for processing.

…As the proposed action would only allow production and grow-out of AquAdvantage Salmon at facilities outside of the United States, the areas of the local surrounding environments that are most likely to be affected by the action lie largely within the sovereign authority of other countries (i.e., Canada and Panama).

Because NEPA [the National Environmental Policy Act] does not require an analysis of environmental effects in foreign sovereign countries, effects on the local environments of Canada and Panama have not been considered and evaluated in this draft EA except insofar as it was necessary to do so in order to determine whether there would be significant effects on the environment of the United States….

In addition, social, economic and cultural effects of the proposed action on the United States have not been analyzed and evaluated because the analysis in this draft EA preliminarily indicates that the proposed action will not significantly affect the physical environment of the United States.

If I am getting this right, the FDA is saying that since the salmon is being raised elsewhere, it’s OK to produce it.

This report is generally interpreted as opening the door to marketing of GM salmon within the United States, and soon.

Will it be labeled as such?  I suppose that too is up to Canada and Panama.

Revisit patent protection anyone?

Dec 22 2012

All you need is a rutabaga and a dream

I’m just back from attending the 15th annual International Rutabaga Curling Championship at the Farmers’ Market in  upstate Ithaca, New York.

This year’s championship event took place, as always, on the last day of the farmers’ market season.

Rutabagas, for the unitiated, are root vegetables of the Brassica family, most likely originating as a cross between a turnip and a cabbage.

Unlovely as they may be, rutabagas are just right for rolling down an icy lane (you can cook and eat them afterwards).

Before the festivities begin, the chorus does a quick rehearsal, this one filmed by a Japanese photographer for a reality show of unusual sporting events.  The program sent a crew to participate, making this a truly international event.

The event has its own original song, Joe Crookston’s The Rutabaga Curl.

But beyond the sport, the high point is always the sing-along rendition of the Rutabaga Chorus.   Its words are explained as the original lyrics for a tune later repurposed for Handel’s Messiah.

My favorite line: “Re-peat re-frain forever and eeeeever….”

Happy holidays!