Rough draft

While we would think government agencies has it in their best interest to protect us, consumers, humans and animals in what we eat; it is evident that this is not the case due to outdated policy and the overlooks in our food system. Although agencies such as the FDA and USDA have a set of jurisdictions, they do not exercise their authority in situations that matter the most. A huge flaw within the system starts with the FDA and their approval of corn, feathers, and antibiotics in animal feed.

This is a topic that concerns all consumers in the United States. We often overlook even such issues because we place our trust in the government and believe that they serve in our best interest because after all we did elect these officials. This article will take you behind the scenes of the food industry and the United States’ government oversight and outdated policy on the topic of food safety.

According to Marion Nestle, Paulette Goddard Professor of Nutrition, Food Studies and Public Health at NYU, prior to the late 1800’s, the U.S government took no responsibility for food safety. They were forced to do so by public demands that sparked from journalists frequent visits to slaughterhouses who shared their experiences. This outraged caused Congress to pass a Meat Inspection Act in 1890 that authorized inspection of salt pork, bacon, and pigs intended for export. A drastic blow to the food industry and the government came in 1906 when Upton Sinclair published his expose in the meat industry, specifically the Chicago stockyards. Following the confirmation of these alligations proposed by Sinclair, Congress immediately passed two separate pieces of legislation: the Pure Food and Drug Act and the Meat Inspection Act, both in 1906. Interesting how secret investigations have to be done and publicized to force our government to want to get its act together isn’t it? This is only the start of the problem.

The Food and Drug Administration formed in 1906, the same year Sinclair released his expose, is a federal agency responsible for protecting public health by assuring safety and security of human and animal drugs, biological products, medical services, OUR NATION’S FOOD SUPPLY (this includes food additives), cosmetics and products that admit radiation. Consumer Reports article, “You are what they eat,” does not hold back and immediately claims that the “federal government isn’t doing enough to protect the feed supply.” They even assert that some regulatory loopholes could allow mad cow infection. The article informs us that the FDA delegated much enforcement responsibility to the states, which conduct 70% of feed-company and renderer inspections. This means that the FDA hands over its responsibility to assure not only our safety but animal safety over to state legislatures. While 70 to 90% of cattle and chicken feed is plant based: corn and soybean meal, the remaining 10 to 30% remains questionable. Processed feathers and poultry litter are acceptable sources of protein in cattle feed according to the FDA. Farmed fish may be given rendered meat, bone and feather meal. The ultimate goal is to fatten animals as fast and cheaply as possible. Also included in feed are medications given routinely to animals even the healthy ones in order to boost growth and minimize infections. Nestle also takes a stance on mediciations, specifically antibitoics. Antibiotics are chemicals that prevent bacteria from reproducing, when added to animal food or water they tend to grow faster and need less feed. Antibiotic-resistant baateria survives and multiplies causing potential health problems for our animals. In 1977, the FDA proposed to restrict the use of antibiotics in animal feed but was overruled by Congress under pressure received from farm-state lawmakers, livestock producers, and makers of the drug. One might think to go organic but what does “organic” really mean?

In his piece, “Organic Illusions,” Blake Hurst, Missouri Farm Bureau’s Board of Directors president acknowledges the organic process. According to a Stanford study organic foods were less likely than conventional foods to have pesticide residues, while organic foods were higher in E.Coli. E.Coli is able to accept genes from related bacterial species to form “stable variants” that can pass the borrowed genes along to other bacteria as they divide and multitply. The E. Coli variant known as O157:H7 is especially dangerous, it picks up Shigella gene for a toxin that destroys  red blood cells and includes a syndrome of bloddy diarrhea, kidney failure, and death (Marian Nestle, “Resisting Food Safety, 41). He questions whether the organic food consumer’s purchase is actually organic because there is no testing done to check. He argues organic foods are labeled organic because producers certify that they’ve followed organic procedures.Yet again, here is evidence of government oversight where they trust that producers are honest when they say that their foods are organic because of procedures that were followed. Who is to say if these foods are honestly organic? How will consumers know if these producers are telling them the truth or robbing them for their buck?

Nestle argues that by switching to hay there is a 1% chance of an E. Coli presence, which is more appealing to the health on consumer. Meat producers are not likely to favor these approaches because they are concerned about putting the maximum weight on their animals, and drug producers are still concerned with selling antibiotics to meat producers. Consumer reports argues that animals being raised and fed organic feed would be safer for our food supply in some ways, but there is no guarantee that organic feed is free of garden variety bacteria including salmonella. The alternatives are presented, it is just a matter of producers being willing to accept them.

Should the FDA consider a new proposal for the restriction of animal feed? Or on a simplier note, is the FDA worthy of our trust? 700 FDA inspectors must oversee 30,000 manufacturers and processors, 20,000 warehouses, 785,000 commercial and institutional food establishments, 128,000 grocery and convenience stores, and 1.5 million vending operations. They only conduct 5,000 inspections annually, visited less than 2% ofthe places under their jurisdiction and inspected less than 1%  of imported foods prior to 2001.

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