Civil Eats

The U.S. Food and Drug Administration is taking its biggest step yet to rein in the indiscriminate use of antibiotics that help food animals grow bigger, faster. The agency said Wednesday it is asking veterinary drug makers to voluntarily phase out medically important drugs from being available over the counter in the hope that the shift will help combat growing antimicrobial resistance.

Under FDA’s proposal, these antimicrobials will still be allowed in animal agriculture but, if veterinary drug companies agree to change the labels, farmers will be allowed to use the drugs only to prevent, control, or treat diseases and under the supervision of a veterinarian and not for promoting growth or improving feed efficiency.

The agency said it was taking the voluntary action to “preserve the effectiveness of medically important antimicrobials for treating disease in humans.” Read More

The Just Label It (JLI) Campaign announced today that a record-breaking one million Americans of all political persuasions have called on the FDA to label genetically engineered (GE) foods. Today, March 27, is the date that the FDA is required to respond to the petition. It took JLI and its more than 500 partner organizations less than 180 days to accumulate an historic number of public comments—a testament to the power of collective voices to demand our right to know what’s in our food. (I’ve written about the campaign before here, here, and here.) Read More

It looks like 2012 will be the year of two salmons: one a genetically altered “Frankenfish” currently under review by the Food and Drug Administration, and the other an inhabitant of one of the world’s last great wild salmon runs, which is unfortunately situated atop a whole lot of copper and gold deposits. Read More

According to recent numbers, 80 percent of antibiotics on the market today are being administered to animals, much of which is given non-therapeutically to promote growth. A new report today on msnbc.com by Helena Bottemiller reveals that ractopamine hydrochloride, a growth promoting drug, has become the focus of an international trade dispute concerning its potential effects on human health.

“Although few Americans outside of the livestock industry have ever heard of ractopamine, the drug is controversial,” Bottemiller writes. “Fed to an estimated 60 to 80 percent of pigs in the United States, it has sickened or killed more of them than any other livestock drug on the market, Food and Drug Administration records show. Cattle and turkeys have also suffered high numbers of illnesses from the drug.”

According to the story, USDA meat inspectors have reported an increase in “downer pigs”–livestock that is unable to walk–who have been fed ractopamine. On Monday, the Supreme Court unanimously voted down a California ban on “downer” livestock being used in the food supply, on the basis of a federal preemption. Read More

The Food and Drug Administration announced Wednesday that it will be restricting the use of cephalosporin–a type of antibiotic–in food animals in order to prevent the growth of antibiotic-resistant strains of human diseases. Read More

The Food and Drug Administration (FDA) pulled a Scrooge move just before Christmas. The agency published an entry in the Federal Register declaring that it will end its attempt at mandatory restrictions on the use of antibiotics in animal agriculture. The agency isn’t advertising the shift, though: This news would have remained a secret if not for Maryn McKenna’s Superbug blog over at Wired. McKenna, who specializes in writing about antibiotics and their link to pathogens, caught the Federal Register notice.

This is a sorry end to a process that began in 1977 (!), but McKenna created an excellent timeline that traces the history of the issue back to the 1950s. In 2009, the Obama administration breathed new life into a moribund process because the top two Obama appointees at the FDA, Commissioner Margaret Hamburg and her then-deputy Joshua Sharfstein, strongly supported restricting antibiotic use in agriculture.

But despite Hamburg and Sharfstein’s many supportive statements, the FDA has only produced a draft set of “voluntary” guidelines. And, with this latest announcement, it looks like that’s as far as they’re willing to go. Read More

On Monday afternoon a coalition of 11 food safety, environmental, consumer and fisheries organizations sent a letter to the U.S. Food & Drug Administration (FDA) calling for a halt to its approval of a genetically engineered (GE) salmon after learning that the company’s–AquaBounty Technologies, Inc.–research site was contaminated with a new strain of Infectious Salmon Anaemia (ISA), the deadly fish flu that is devastating fish stocks around the world. Read More

Today, a broadbased coalition of nearly 400 businesses and organizations dedicated to food safety and consumer rights called on the U.S. Food and Drug Administration (FDA) to require labeling of genetically engineered (GE) foods, to give consumers the right to know what is in our food. The Just Label It – We Have a Right to Know campaign submitted a petition on behalf of millions of consumers to the FDA calling for the mandatory labeling of GE foods, also referred to as genetically modified organisms, or GMOs. These are foods that are altered at the molecular level in ways that could not happen naturally. Read More

Back in March, Tom Philpott wrote about the “insane” practice of feeding factory-farmed chickens arsenic:

The idea is that it makes them grow faster — fast growth being the supreme goal of factory animal farming — and helps control a common intestinal disease called coccidiosis.The industry emphasizes that the arsenic is applied in organic form, which isn’t immediately toxic. “Organic” in the chemistry sense, that is, not the agricultural sense — i.e., molecules containing carbon atoms as well as arsenic. Trouble is, arsenic shifts from organic to inorganic rather easily. Indeed, “arsenic in poultry manure is rapidly converted into an inorganic form that is highly water soluble and capable of moving into surface and ground water,” write Keeve E. Nachman and Robert S. Lawrence of the Johns Hopkins Center for a Livable Future.

Inorganic arsenic is the highly poisonous stuff — see the absurd and wonderful Cary Grant classic Arsenic and Old Lace, or the EPA’s less whimsical take here and here [PDF]. The fact that the organic arsenic added to feed turns inorganic when it makes its way into manure is chilling, given the mountains of concentrated waste generated by factory poultry farms.

One way farmers add arsenic to chicken feed is through drugs such as Pfizer’s Roxarsone. And the industry has (as with most of its worst practices) strenuously defended the use of such additives. While the USDA has by and large ignored the risks (mostly in the form of an unwillingness to look for arsenic in chicken), finally–astonishingly–the Food and Drug Administration (FDA) has acted. Read More

Many Americans, including a high number living in low-income communities, have come to rely on canned tomato sauces, soups, and vegetables to expedite their meal preparations. Yet a new study from the U.S. Food and Drug Administration (FDA) reveals that the canned food items on your dinner plate are over 90 percent likely to be tainted with Bisphenol-A (BPA), a primary chemical used in the lining of cans. (For more information on BPA, check out Civil Eats’ previous reporting here, here, here, and here.)

These findings are notable because they underline the fact that BPA levels in cans are variable depending on the type of food, or even within batches of the same food item. This is the FDA’s largest study to date across a wide spectrum of commonly consumed canned food items, including soups, chilis, pasta and pork and beans–foods often consumed by children, who have a heightened risk of exposure due to their body size. Read More

Chemicals and additives found in the food supply and other consumer products are making headlines regularly as more and more groups  raise concern over the safety of these substances. In a statement released yesterday, the American Academy of Pediatrics (AAP) asked for reform to the Toxic Substances Control Act of 1976. The group is particularly concerned about the effects these substances have on children and babies.

Last month, the U.S. Food & Drug Administration (FDA) held hearings on the safety of food dyes but failed to make a definitive ruling—the most recent study on Bisphenol-A (BPA) added to growing doubts about its safety but the FDA’s stance remains ambiguous. Meanwhile, in 2010, the Government Accountability Office (GAO) reported that the FDA is not ensuring the safety of many chemicals.

Yet while the FDA drags its heels and hedges on the safety of these substances, Americans are exposed to untested combinations of food additives, dyes, preservatives, and chemicals on a daily basis. Indeed, for the vast majority of Americans consuming industrial foods, a veritable chemical cocktail enters their bodies every day and according to the GAO report, “FDA is not systematically ensuring the continued safety of current GRAS substances.” Read More

Consumer Reports’ latest tests of 42 samples from cans and pouches of tuna bought primarily in the New York metropolitan area and online confirm that white (albacore) tuna usually contains far more mercury than light tuna. According to Consumers Union, pregnant women should avoid tuna and younger women and kids should limit their consumption. Read More

The genetically modified salmon called AquAdvantage was discussed on Monday in front of the Veterinary Medicine Advisory Committee, which will help the Food and Drug Administration (FDA) decide whether or not to approve the fish for commercial production. The meeting comes after an unusually short 14-day period of public comment on the “new animal drug.” Read More

When the FDA announced it found the genetically engineered AquAdvantage salmon safe just before Labor Day, news headlines and even Alaska Senator Mark Begich called it a “frankenfish.” A closer look at AquAdvantage makes it seem unlikely that Mary Shelley could have ever dreamed up anything as wild as the fast growing GE salmon. Even more worrisome is the science used to justify the salmon’s safety, which Consumers Union senior scientist Michael Hansen calls “sloppy,” “misleading,” and “woefully inadequate.”

If approved, AquAdvantage will be the first genetically engineered animal to directly enter the U.S. food supply — a fact that raises the stakes of the FDA’s approval process, as it sets a precedent for all future GE animals. Read More

As consumers scramble to check their egg cartons and federal officials investigate two Iowa farms at the center of a half-billion egg recall, it’s becoming clear that no one was overseeing egg safety in Iowa. Read More

The FDA took a significant step yesterday toward restricting the routine feeding of subtherapeutic (medically unnecessary) doses of antibiotics to livestock. As Grist has detailed in previous coverage, this practice — which by some estimates consumes nearly 70% of all antibiotics administered in the U.S. –  has been linked to the rise of antibiotic resistance, both in common pathogens such as salmonella and in previously rare ones such as MRSA. Read More

Consumers Union, the nonprofit publisher of Consumer Reports, and more than 80 farmers, public health, environmental, and organic food organizations today sent a letter to Michael R. Taylor, Deputy Commissioner for Food at the U.S. Food and Drug Administration (FDA), and to Kathleen Merrigan, Deputy Secretary at the U.S. Department of Agriculture (USDA), expressing serious concerns that a proposed U.S. position on food labeling would create major problems for American producers who want to label their products as free of genetically modified (GM)/genetically engineered (GE) ingredients. A copy of the letter can be found online [PDF]. Read More

CBS Evening News’ Katie Couric spoke with former FDA Commissioner and author of The End of Overeating, Dr. David Kessler, and Fast Food Nation author Eric Schlosser for her online discussion this week, called @KatieCouric. The topics ranged from portion sizes to school food, the push back from industry on Couric’s segment last week on non-therapeutic antibiotic use in agriculture, and to other issues of food policy and food safety. The discussion is nearly fifty minutes long, and well worth watching. Here are a few highlights: Read More

There have indeed been studies that have indicated genetically engineered crops like corn and soy might negatively affect our health. Most of these studies conclude by saying “more study is needed” — but further study never happens because Monsanto, which owns the patents of most GMO seeds simply won’t give them to independent researchers for scientific use without onerous restrictions. The federal government has been no help because under industry pressure the EPA and the FDA ruled back in the 1990s that GMO crops are “substantially equivalent” to their conventional brethren and they have shown no interest in re-opening the GMO can of worms. Read More

On June 12, 1957, Surgeon General Leroy E. Burney stated that “evidence pointed to a causal relationship between smoking and lung cancer,” thereby changing the official position of the United States Public Health Service. This small but significant move opened the door to regulation of Big Tobacco, beginning a battle that came to a head last week with the FDA being granted the most power over the industry to date.

Now, more than a half a century after that first declaration, that same date brought the movie Food, Inc. to theaters, a film that reveals the dysfunction of our food system. With obesity rates at the highest point in history, contaminated food regularly sickening thousands, and government estimating we will continue to spend 6.2% more on healthcare annually (this year, an additional $200 billion, more than our annual economic growth of 4.1%), it is clear that we have a problem as big as smoking: an addiction to cheap, unhealthy food perpetuated by an industry intent on maximizing profits at the expense of our health and our land. It is time to regulate Big Food by changing the culture in Washington that allowed it to proliferate. Read More

The House Energy and Commerce Subcommittee on Health yesterday approved the Food Safety Enhancement Act of 2009, sending the bill to the full committee for a vote expected next week.

The legislation is set to increase the authority and funding of the U.S. Food and Drug Administration, and at yesterday’s markup, Democrats agreed to halve the registration fee all food producers (domestic and foreign) would have to pay from the proposed amount of $1,000 to $500. The $1,000 charge, which had been supported by new FDA Commissioner Margaret Hamburg, would have generated an estimated $378 million—money Democratic lawmakers said would go toward increasing plant inspections and other food safety activities. Read More

UPDATE: Emails show that the FDA relied heavily on the industry for science on BPA.

Chicago is the first city in the nation to ban bisphenol A (BPA) from plastic baby bottles and sippy cups for children under the age of 3. The Chicago City Council voted to approve the ban yesterday, which would be implemented early next year, and Mayor Richard Daley said he will sign the ordinance. “The F.D.A. continues to be recalcitrant and very slow about taking any action on BPA,” said Chicago Alderman Manuel Flores, one of two city officials who proposed the ban last year, after hearing concerns about the potentially harmful effects of the chemical to young children. Read More

In an attempt to reclaim its reputation a few months back, the makers of High Fructose Corn Syrup (HFCS) created a few sneaky commercials, which were really hard for us in the food community to take seriously.   But now HFCS is in the news again — and this time the reason is much worse. It turns out that many foods sweetened with HFCS contain mercury, left as a residue in the production of caustic soda, a key ingredient in HFCS.  And worst of all, the FDA and the industry have known about this potential toxin and has continued serving it up since at least 2005. Read More

Two weeks ago, the Food and Drug Administration declared a natural zero-calorie sweetener derived from the herb stevia safe for use in foods and beverages, clearing a path for Coca-Cola, PepsiCo and other companies to market it in a variety of products. A long time favorite of natural food lovers, stevia is a shrub native to South America and has 30–45 times the sweetness of ordinary table sugar. Widely available for years in Brazil, China and Japan (they use it in their version of Coke), stevia is banned for use in food in the European Union. Read More

According to a Consumer Reports poll released this week, Americans are becoming increasingly concerned about U.S. food safety, and the overwhelming majority want the government to do more to monitor the American food supply. Read More