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The Cornucopia Institute

Yesterday, the Food and Drug Administration (FDA) released a draft guidance document to clarify how egg producers, including organic farmers with outdoor access, can comply with its 2009 egg safety rule aimed at reducing salmonella contamination in the nation’s egg supply.

Since organic producers are required by federal standards to grant outdoor access to their laying hens, the guidance applies to all organic egg producers. The FDA, which collaborated with the U.S. Department of Agriculture's (USDA) National Organic Program in promulgating their guidance, recognizes minute covered porches—which do not afford true and meaningful outdoor access to laying hens—as one of four possible organic production systems and thereby legitimizes their use.

Already the focus of controversy and threatened lawsuits, the USDA has been widely criticized for allowing giant “organic” factory farms, confining as many as 100,000 birds to a building, to skirt the requirements for outdoor access by employing tiny screened porches, often with a capacity of only one-three percent of the confined birds. The USDA is currently allowing these giant poultry operations to claim these structures as the legally required “access to the outdoors.”

“This is collusion between two Obama administration agencies to significantly and permanently weaken the integrity of the organic standards,” says Mark Kastel, codirector of The Cornucopia Institute.

“By giving the OK to use covered porches as ‘outdoor access,’ and putting additional burdens on producers with legitimate outdoor runs or pasture, the recommendations in this food safety document decisively tilt the playing field to industrial-scale producers,” added Kastel.

Some in the organic community had been concerned that the FDA would require impractical swabbing and disinfecting of the outdoor areas but the draft guidance puts these concerns to rest.

However, other prevention and control measures that are included in the guidance could force organic producers to devote significant additional resources, or may even make it impossible for pastured poultry operations to comply.

Stephanie Alexandre, a producer of certified organic, pastured eggs near Crescent City, CA, objects to the draft guidance.

“It’s ironic that federal regulators would apply such scrutiny, and costly and labor-intensive requirements, to my farm when there is abundant published, peer-reviewed research indicating that the real danger to society, from salmonella contamination in eggs, comes from giant industrial operations, generally with caged birds, not with modest sized flocks of pastured poultry,” said Alexandre.

For example, despite weak scientific evidence that contact with wild birds is a significant risk factor for salmonella contamination, the FDA requires organic producers to minimize contact with other birds. The agency recommends noise cannons, temporary confinement, netting, or even structures with roofs (porches) which would be cost prohibitive for most organic producers with meaningful outdoor access.

Some of the recommended measures would discourage chickens from using the outdoor space. For example, while noise cannons would be effective in scaring wild birds, they would also scare the laying hens and effectively make the outdoor area an inhospitable environment for the organic birds.

“In effect, the FDA’s proposed recommendations would steer organic egg producers toward the use of porches, which would be the most effective and cost-efficient way to ensure complete compliance with the rule,” Kastel explained. “Why would farm operators invest the extra labor and expense to meet the FDA requirements, and put their birds outside, when they can create a token structure, attached to their main building, and continue to confine their animals?”

“The recommendations in this draft guidance essentially give organic producers a textbook of excuses for why their birds can legally be confined in industrial settings,” says Kastel. “To create the safest and most nutritious eggs, we should be encouraging more and better use of outdoor space for laying hens so that they can exhibit their true, native behavior. But this FDA document does just the opposite.”

The Cornucopia Institute was already investigating a legal action against the USDA for its unwillingness to enforce the law requiring outdoor access for chickens. It is the farm policy organization’s contention that confining birds to small adjacent structures on massive industrial-scale “farms,” does not meet the federal legal mandate.

In what now appears to be a cynical ploy, the USDA had asked the National Organic Standards Board (NOSB)—the expert citizen panel that Congress created to advise the Secretary of Agriculture—to develop standards to help enforce the requirement for outdoor access.

The NOSB completed a years-long process of collaborating with industry representatives and forwarded a series of recommendations to USDA leadership that would have required a minimum amount of square footage, and other requirements, like the number and size of doors, that would have facilitated enforcement of the outdoor access provisions.

Recently, leadership at the USDA’s National Organic Program informed organic stakeholders that they would not follow through with amending poultry/livestock regulations, incorporating the NOSB’s recommendations, because it was currently “not a priority.”

“The lack of enforcement action by the USDA has helped shift the lion’s share of production of organic eggs to giant agribusinesses, which mostly produce conventional eggs, at the expense of family-scale farmers who are producing a superior product in an environmentally responsible manner and treating their livestock humanely,” stated Cornucopia’s Kastel.

“We will not stand by while the most dedicated and responsible, and law-abiding, organic producers are placed at a competitive disadvantage by the arbitrary and capricious behavior of the current administration’s leadership at the USDA and FDA.”

The FDA has opened a 60-day public comment period for input pursuant to their draft guidance on compliance with the salmonella safety rule for producers with outdoor access for laying hens.

The Cornucopia Institute will soon release an action alert and briefing paper so interested organic stakeholders can make informed comments on the draft guidance.

If organic farmers and consumers interested in protecting the integrity of the organic label, and possibly the country’s safest agricultural producers, are not already Cornucopia members, they can either join by visiting the organization’s website.

Visit EcoWatch’s FACTORY FARMING page for more related news on this topic.

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Center for Food Safety

The Center for Food Safety (CFS) applauded the U.S. Food and Drug Administration (FDA) Jan. 4 for pre-releasing its long awaited prohibition on the extra-label use of cephalosporin drugs in food-producing animals. Cephalosporin drugs are an essential tool in both human and animal medicine, but mounting evidence has linked extra-label use of these drugs to the development and spread of cephalosporin-resistant organisms.

“This is a critical win for consumers, food safety advocates and the medical community,” said Andrew Kimbrell, executive director for the Center for Food Safety. “But it’s high time that FDA wakes up to the dangers that non-therapeutic uses of all antibiotics pose to our health and the safety of our food supply,” Kimbrell said.

Cephalosporins are a vitally important class of antibiotics used most often in the treatment of serious Salmonella infections but also used to treat many other serious infections. The announcement Jan. 4 comes more than three years after the FDA first published an order prohibiting for the extra-label uses in food-producing animals of these drugs. That order was then withdrawn by the FDA before it could go into effect, citing the need for additional review of the public comments it received.

In its notice Jan. 4, FDA said that it plans to publish the Final Rule in the Federal Register on Jan. 6 announcing the prohibition of the extra-label use of cephalosporin drugs in food-producing animals. The Final Rule will go into effect 90 days from being published in the Federal Register and FDA will accept public comments for 60 days following the Federal Register notice. FDA’s Final Rule will continue to allow approved label uses of these drugs for food producing animals as long as they are done in a safe and effective manner.

“The extra-label ban is just the first of many actions that FDA must make in order to better protect the public from the dangers of antibiotic-resistance,” said Paige Tomaselli, staff attorney for the CFS. “Losing the effectiveness of critically important antibiotics as a result of our own misuse would be a catastrophic loss for modern medicine,” added Tomaselli.

In August 2010, more than 180,000 citizens sent letters to the FDA responding to the agency’s request for comments on rules governing the judicious use of antibiotics on industrial farms. Those letters joined dozens of scientific experts and public interest organizations calling on FDA to tighten oversight and curtail misuse and overuse of antibiotics on industrial farms. In its comments to the FDA, CFS thanked FDA for initiating discussion on the critical issue but expressed deep concern that its measures would not be voluntarily implemented and that regulation mandating immediate action is required instead. Further, in the absence of a clear timeline and strict goals, CFS stressed that the agency’s approach lacked the urgency that this critical issue demands.

For more information, click here.

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