Saturday, August 11, 2007

The Double Standard on Trading Contaminated Chinese and US Consumer Products


By Dr. Samuel S. Epstein and Ronnie Cummins
Environmental News Network

Tuesday 31 July 2007

Chicago - The dangers of cheap Chinese exports of contaminated consumer products has received extensive media coverage, besides the formation of a Cabinet-level Product Safety Panel. These exports include personal care products, such as toothpaste contaminated with the anti-freeze diethylene glycol, honey contaminated with dangerous antibiotics, and food contaminated with banned drugs, pesticides and carcinogens. In contrast, Congress and the media remain silent on the export of dangerous U.S. consumer products, besides their decades-old domestic sale.

U.S. personal care and cosmetic products contain a wide range of avoidable toxic ingredients, notably multiple carcinogens, hormones and allergens, which remain unregulated by the FDA. These products include leading brands of toothpaste with carcinogenic ingredients. In sharp contrast, the 30-member state European Union has developed a Cosmetic Directive, which bans the manufacture and import of products suspected of causing harm to human health. Highlighting FDA's indifference is the State of California's 2005 Safe Cosmetic Act, requiring cosmetic companies to disclose information on toxic ingredients.

Of major concern is U.S. milk from cows injected with Monsanto's genetically engineered recombinant bovine growth hormone (rBGH) to increase milk production. According to Monsanto, about one third of dairy cows in the nation are in herds where the hormone is used. This milk contains abnormally high levels of a natural growth factor known as IGF-1. As documented in over 30 scientific publications, detailed in our May 2007 Citizen Petition to the FDA, increased levels of IGF-1 in milk increase risks of breast cancer by up to seven-fold, besides risks of colon and prostate cancers. Not surprisingly, the import of U.S. rBGH dairy products has been banned by Canada, 29 European nations, Norway, Switzerland, Japan, New Zealand, Australia, and South Africa. Also, in June 1999, the United Nations Food Safety Agency, representing 101 nations worldwide, voted unanimously to reject a safety standard for rBGH milk. Nevertheless, there are no FDA restrictions on its continued sale in the U.S., nor any requirement for warning labels.

U.S. beef is heavily contaminated with natural or synthetic sex hormones. When U.S. beef cattle enter feedlots, pellets of these hormones are implanted under the ear skin, a process repeated at the midpoint of their 100-day pre-slaughter fattening period. These hormones increase carcass weight, adding about $80 profit per animal. Not surprisingly, but contrary to the claims of the FDA and USDA, residues of these hormones in meat are up to 20-fold higher than normal. Increased levels of sex hormones are linked to the escalating incidence of reproductive cancers in the U.S. since 1975, 36% for post-menopausal breast cancer, 50% for testicular cancer, and 88% for prostate cancer. Based on these concerns, Europe banned imports of U.S. beef in 1989, and Japan followed up with its own ban in 2003. Before the ban, Japan was the most lucrative overseas market for American beef, importing more than $1.5 billion worth in 2003.

These concerns are not new. As evidenced in a series of General Accounting Office investigations and Congressional hearings, FDA registration and residue-tolerance programs and USDA inspections are in near total disarray, aggravated by brazen denials and cover-ups. A January 1986 report, "Human Food Safety and the Regulation of Animal Drugs," unanimously approved by the House Committee on Government Operations, concluded that "the FDA has consistently disregarded its responsibility - has repeatedly put what it perceives are interests of veterinarians and the livestock industry ahead of its legal obligation to protect consumers - jeopardizing the health and safety of consumers of meat, milk and poultry."


Talk to the authors: Samuel S. Epstein, M.D., Professor emeritus, Environmental & Occupational Medicine, University of Illinois at Chicago School of Public Health, Chairman of Cancer Prevention Coalition, 312-996-2297 epstein@uic.edu. Ronnie Cummins, National Director of Organic Consumers Association, 218-349-3836 ronnie@organicconsumers.org.


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FDA Suspends Plan to Close Many of Its Field Laboratories
The Associated Press

Thursday 02 August 2007

Washington - The Food and Drug Administration's commissioner said Wednesday that he had suspended plans to close more than half the agency's field laboratories.

The commissioner, Dr. Andrew C. von Eschenbach, is awaiting recommendations from a presidential panel about how to better guarantee the safety of imported food and other products.

He said Wednesday that he wanted to make sure the F.D.A. was "doing the right thing and doing it in the right way" before proceeding.

President Bush established the Import Safety Working Group on July 18 and asked for recommendations in 60 days.

"Once we have the benefit of that information, we can come back again to the more fundamental question of how do we create a field operation that is adapted to and equipped to manage the converging challenges and converging complexities of our ability to ensure the quality of the products that F.D.A. regulates," Dr. von Eschenbach said.

The panel was created after a spate of recalls of imported food and consumer products, many of them Chinese and regulated by the F.D.A.

Against that backdrop, the F.D.A. has said it wants to consolidate its lab network to modernize its food safety efforts. Lawmakers, some lab employees and the union that represents much of the F.D.A. work force contend that would make matters worse.

In a letter sent to Dr. von Eschenbach on Tuesday, John D. Dingell and Bart Stupak, both Democratic representatives from Michigan, asked if the purpose of the lab closings was to privatize the testing of imported foods. They cited a pilot program to assess doing just that.

Dr. von Eschenbach denied that the closings were part of an outsourcing plan. Later, however, he said the agency would consider certifying or granting credentials to private labs to do some testing work. He further suggested that the F.D.A. could collaborate more with Customs and Border Protection and the states in policing imports.

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