Food safety in the United States relates to the processing, packaging, and storage of food in a way that prevents food-borne illness within the United States. [1] The beginning of regulation on food safety in the United States started in the early 1900s, when several outbreaks sparked the need for litigation managing food in the food industry. Over the next few decades, the United States created several government agencies in an effort to better understand contaminants in food and to regulate these impurities. Many laws regarding food safety in the United States have been created and amended since the beginning of the 1900s. Food makers and their products are inspected and regulated by the Food and Drug Administration and the Department of Agriculture.
The United States has recently taken food safety into consideration again after several deadly outbreaks occurred in the early 2000s. Incidents such as the E.coli contaminated spinach in 2006 bring attention to the regulation surrounding the food industry and food quality control. Many outbreaks have occurred because of loose enforcement of regulation and lack of quality testing of every batch of food that is being produced. Most legislation regarding food safety is in the wake of a deadly outbreak of a food-borne illness. The bacteria and viruses that cause most of the food-borne illnesses are Salmonella , E. coli , Listeria , norovirus, Campylobacter , and Clostridium perfringens . [2] These can lead to some deadly diseases that have killed many people in the United States.
Food safety in the United States is necessary in order to prevent and properly report food-borne illnesses. [3] In 2011, a total of 9.4 million incidents of food-borne illness occurred in the United States. [4] Widespread food-borne outbreaks typically spark legislation rather than legislation working as a preventative measure against food-borne illnesses.
Prior to 1906, there were no laws related to food and intentional additives and unintentional contaminants added to food. The Jungle , a novel published by Upton Sinclair in 1905, described the horrible working conditions in the meat-packing industry. His detailed account of the low quality of meat caused outrage among the public. [5]
In 1906, two acts were signed into law following the aftermath of the accounts of lack of food quality: the Pure Food and Drug Act and the Federal Meat Inspection Act. [6] The Pure Food and Drug Act forced food manufacturers to only sell unadulterated foods and to correctly label foods. The Meat Inspection Act lead to the creation of the US Department of Agriculture's Food Safety and Inspection Service, which manages the production of meat, poultry, and eggs, enforcing regulated limits of certain contaminants and enforcing quality of product. [7] These laws have become a foundation for food safety in the United States and have set a precedent in regulating food. Since these two acts were signed, amendments and changes have taken place, but upon the framework set by the Pure Food and Drug Act and the Meat Inspection Act. These acts allowed U.S. court case called U.S. vs. 95 Barrels Alleged Apple Cider Vinegar to rule that the apple cider vinegar in question was misbranded as it was made from dried apples instead of fresh apples.
Recent legislation regarding food safety includes the Food Safety Modernization Act (FSMA), signed into law on January 4, 2011, by Barack Obama. [8] This sweeping reform of food safety law shifted the FDA's focus from responding to contamination to preventing it. [9] The FDA was tasked with strengthening regulations regarding produce safety, as well as regulations with increased preventative control measures in facilities that process food. [10] FSMA's Produce Safety Rule (PSR), which went into effect on January 26, 2016, and is now being rolled out and implemented in different states, [11] establishes minimum standards for the safe growing, harvesting, packing, and holding of fruits and vegetables grown for human consumption. [12]
The United States has three federal and two state governmental organizations that are in control of food safety within the United States: the Food and Drug Administration (FDA), the Food Safety and Inspection Service (FSIS), the Center for Disease Control and Prevention (CDC), the State Department of Public Health, and the State Department of Agriculture. [13] These organizations focus on the production and distribution of food, making sure all food distributed to retail stores, restaurants, and consumers is safe, without contamination from food-borne illness. While there are many other smaller organizations that participate in the distribution of safe food, these organizations are the most active in regulating food and preventing food-borne illness in the United States.
In 1862, the government division called the Bureau of Chemistry was created. [14] The Bureau of Chemistry separated into two divisions in 1927, one of which was called the Food and Drug Administration (FDA). [15] As a new organization, the FDA had little legal control when enforcing the few regulatory food safety laws. However, an incident in the late 1930s improved the FDA's control over food and drugs.
In the 1930s, a new antibacterial drug called sulfanilamide was synthesized and was widely accepted. One chemist at S.E. Massengill Co. in Bristol, Tennessee wanted to come up with a way to liquify the insoluble drug so children and adults could take the drug in liquid form. Diethylene glycol (DEG) was used to dissolve the drug, even though DEG is deadly to humans. Without any toxicologic testing, 1300 bottles of this "Elixir Sulfanilamide" were distributed to consumers and physicians. As soon as people starting dying after taking the elixir, the drug was recalled. The FDA investigated the company and found no clinical trials and no evidence of further testing involve the elixir.
At this time the FDA had no authority to penalize the company in question. Charges against the owner were filled, and six months later, a law called the Food, Drug, and Cosmetic Act of 1938 was signed. This law forced all new food, drugs, and cosmetics to be certified by the FDA before being put on the market. [16] This act granted the FDA with enforcing and legal power that has helped regulate food and drugs ever since.
As of 2018, the FDA regulates more than $2.5 trillion in consumer food, medical products, and tobacco in the United States. [17] The head of the FDA has the position of Commissioner of the FDA. The FDA is currently in the government branch of the United States Secretary of Health and Human Services.
The 25 percent of food that the FDA does not regulate is monitored instead by the Food Safety and Inspection Service (FSIS) and includes all egg, meat, and poultry products processed and distributed in the United States. [17] FSIS was founded upon the creation of the Federal Meat Inspection Act of 1906, the Poultry Products Inspection Act of 1957, and the Egg Products Inspection Act of 1970, along with several amendments to these acts that have been passed. [18] FSIS enforces safe, wholesome, correctly-labeled egg, poultry, and meat products in every state in the United States including Puerto Rico. [18] Currently, FSIS is an agency in the United States Department of Agriculture.
In 1948, the Malaria Control in War Areas, a program run by the U.S. Public Health Service, was turned into the Communicable Disease Center (CDC). On July 1, the CDC was established in Atlanta, Georgia. One of the CDC's initial goals was to eradicate malaria from the United States entirely, which it successfully accomplished in 1951. [19] When polio starting spreading in the 1950s, the CDC started to develop surveillance methods to keep track and record incidents of polio to help fight the spread of the paralytic and deadly virus. By the 1970s, less than 10 people had contracted polio in the United States. [20] In the 1970s, when the CDC's name changed to the Center for Disease Control (CDC), the organization continued to advocate for other diseases and urgent public health issues. [21] In 2016, when the Zika virus spread to the United States, the CDC immediately mobilized their Emergency Operations Center and took appropriate action. [19] The main goal of the CDC is to keep track of health, safety, and security threats to the American people.
Before 1906, there were no laws concerning food safety and regulating how food is produced, manufactured, and distributed. Laws are typically written in the wake of severe outbreaks, rather than as a preventative measure. The current food safety laws are enforced by the FDA and FSIS. The FDA regulates all food manufactured in the United States, with the exception of the meat, poultry, and egg products that are regulated by FSIS. [15] The following is a list of all food safety acts, amendments, and laws put into place in the United States. [22] [14]
1906: Pure Food and Drugs Act
1906: Federal Meat Inspection Act
1913: Gould Amendment
1930: McNary-Mapes Amendment
1938: Federal Food, Drug, and Cosmetic Act
1948: Miller Amendment
1953: Factory Inspection Amendment
1954: Miller Pesticide Amendment
1957: Poultry Products Inspection Act
1958: Food Additives Amendment
1960: Color Additive Amendment
1962: Talmidge/Aujeb Act
1966: Fair Packaging and Labeling Act
1967: Wholesome Meat Act
1968: Wholesome Poultry Products Act
1968: Animal Drug Amendments
1970: Egg Products Inspection Act
1976: Vitamins and Minerals Amendment
1980: Instant Formula Act
1990: Sanitary Food Transportation Act of 1990
1990: Nutrition Labeling and Education Act
1990: Organic Foods Production Act
1994: Dietary Supplement Health and Education Act
1996: Federal Tea Tasters Repeal Act
1996: Food Quality Protection Act
1997: FDA Modernization Act
1997: National Economic Crossroads Transportation Efficiency Act
2002: Public Health Security and Bioterrorism Preparedness and Response Act
2002: Farm Security and Rural Investment Act
2003: Animal Drug User Fee Act
2004: Passage of the Food Allergy Labeling and Consumer Protection Act
2005: Sanitary Food Transportation Act
2011: Food Safety Modernization Act
2016: Agriculture Marketing Act
Listed are the deadliest incidents of food-borne illness in the past few decades:
1992–1993 – Jack in the Box E. coli outbreak: Beef patties distributed by Jack in the Box restaurants were contaminated with E. coli O15:H7. Investigators say 602 patients were infected with E. coli, 144 people were hospitalized, and three people died. [23]
2003 – Chi Chi's Green Onion Hepatitis A outbreak: Green onions produced in Mexico were unknowingly infected with hepatitis A. These onions were served raw at a select Chi Chi restaurant near Pittsburgh, Pennsylvania. Of the 575 people who caught the disease, three people died. [24]
2006 – Dole Baby Spinach E. coli outbreak: Baby spinach packaged in Dole's freshly bagged spinach was contaminated by the spinach field's proximity to cattle ranches. There were 238 who fell ill, of which 103 were hospitalized, and five people died. [25]
2008 – King Nut Peanut Butter Salmonella outbreak: The King Nut creamy peanut butter was the source of a Salmonella outbreak throughout the United States with 714 total infected and a death toll of nine. [26]
2011 – Cantaloupe listeriosis outbreak: Whole cantaloupes grown at Jensen Farms in Granada, Colorado were found to be contaminated with Listeria monocytogenes, a bacterium that causes listeriosis. The outbreak caused a total of 33 deaths from the 147 infected patients. [27]
2015–2016 – Cucumber Salmonella outbreak: Investigators found Salmonella in cucumbers grown in Baja, Mexico and distributed by Andrew and Williamson Fresh produce. Of the 907 people infected with Salmonella, 204 were hospitalized, and six people died.
Foodborne illness is any illness resulting from the contamination of food by pathogenic bacteria, viruses, or parasites, as well as prions, and toxins such as aflatoxins in peanuts, poisonous mushrooms, and various species of beans that have not been boiled for at least 10 minutes.
Salmonellosis is a symptomatic infection caused by bacteria of the Salmonella type. It is the most common disease to be known as food poisoning, these are defined as diseases, usually either infectious or toxic in nature, caused by agents that enter the body through the ingestion of food. In humans, the most common symptoms are diarrhea, fever, abdominal cramps, and vomiting. Symptoms typically occur between 12 hours and 36 hours after exposure, and last from two to seven days. Occasionally more significant disease can result in dehydration. The old, young, and others with a weakened immune system are more likely to develop severe disease. Specific types of Salmonella can result in typhoid fever or paratyphoid fever. Typhoid fever and paratyphoid fever are specific types of salmonellosis, known collectively as enteric fever, and are, respectively, caused by salmonella typhi and paratyphi bacteria, which are only found in humans. Most commonly, salmonellosis cases arise from salmonella bacteria from animals, and chicken is a major source for these infections.
Food policy is the area of public policy concerning how food is produced, processed, distributed, purchased, or provided. Food policies are designed to influence the operation of the food and agriculture system balanced with ensuring human health needs. This often includes decision-making around production and processing techniques, marketing, availability, utilization, and consumption of food, in the interest of meeting or furthering social objectives. Food policy can be promulgated on any level, from local to global, and by a government agency, business, or organization. Food policymakers engage in activities such as regulation of food-related industries, establishing eligibility standards for food assistance programs for the poor, ensuring safety of the food supply, food labeling, and even the qualifications of a product to be considered organic.
The 2006 North American E. coli outbreak was an Escherichia coli O157:H7 outbreak from prepackaged spinach. The outbreak occurred in September 2006, and its origin was an Angus cattle ranch that had leased land to a spinach grower. At least 276 consumer illnesses and 3 deaths have been attributed as a result from the outbreak.
Food safety is used as a scientific method/discipline describing handling, preparation, and storage of food in ways that prevent foodborne illness. The occurrence of two or more cases of a similar illness resulting from the ingestion of a common food is known as a food-borne disease outbreak. This includes a number of routines that should be followed to avoid potential health hazards. In this way, food safety often overlaps with food defense to prevent harm to consumers. The tracks within this line of thought are safety between industry and the market and then between the market and the consumer. In considering industry-to-market practices, food safety considerations include the origins of food including the practices relating to food labeling, food hygiene, food additives and pesticide residues, as well as policies on biotechnology and food and guidelines for the management of governmental import and export inspection and certification systems for foods. In considering market-to-consumer practices, the usual thought is that food ought to be safe in the market and the concern is safe delivery and preparation of the food for the consumer. Food safety, nutrition and food security are closely related. Unhealthy food creates a cycle of disease and malnutrition that affects infants and adults as well.
The Center for Food Safety and Applied Nutrition is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements, and cosmetics, as opposed to drugs, biologics, medical devices, and radiological products, which also fall under the purview of the FDA.
Adulteration is a legal offense and when the food fails to meet the legal standards set by the government, it is said to have been Adulterated Food. One form of adulteration is the addition of another substance to a food item in order to increase the quantity of the food item in raw form or prepared form, which results in the loss of the actual quality of the food item. These substances may be either available food items or non-food items. Among meat and meat products some of the items used to adulterate are water or ice, carcasses, or carcasses of animals other than the animal meant to be consumed. In the case of seafood, adulteration may refer to species substitution (mislabeling), which replaces the species identified on the product label with another species, or undisclosed processing methods, in which treatments such as additives, excessive glazing, or short-weighting are not disclosed to the consumer.
Produce traceability makes it possible to track produce from its point of origin to a retail location where it is purchased by consumers.
Raw meat generally refers to any type of uncooked muscle tissue of an animal used for food. In the meat production industry, the term ‘meat’ refers specifically to mammalian flesh, while the words ‘poultry’ and ‘seafood’ are used to differentiate between the tissue of birds and aquatic creatures.
Michael R. Taylor is an American lawyer who has played leadership roles in the US Food and Drug Administration, agrochemical company Monsanto, and law firm King & Spalding. He currently co-chairs the board of STOP Foodborne Illness, a non-profit that supports victims of serious illness and their families in efforts to strengthen food safety culture and practices in government and industry.
The Food Safety Modernization Act (FSMA) was signed into law by President Barack Obama on January 4, 2011. The FSMA has given the Food and Drug Administration (FDA) new authority to regulate the way foods are grown, harvested and processed. The law grants the FDA a number of new powers, including mandatory recall authority, which the agency had sought for many years. The FSMA requires the FDA to undertake more than a dozen rulemakings and issue at least 10 guidance documents, as well as a host of reports, plans, strategies, standards, notices, and other tasks.
The Food Safety and Inspection Service (FSIS), an agency of the United States Department of Agriculture (USDA), is the public health regulatory agency responsible for ensuring that United States' commercial supply of meat, poultry, and egg products is safe, wholesome, and correctly labeled and packaged. The FSIS draws its authority from the Federal Meat Inspection Act of 1906, the Poultry Products Inspection Act of 1957 and the Egg Products Inspection Act of 1970.
The 1992–1993 Jack in the Box E. coli outbreak occurred when the Escherichia coli O157:H7 bacterium killed four children and infected 732 people across four US states. The outbreak involved 73 Jack in the Box restaurants in California, Idaho, Washington, and Nevada, and has been described as "far and away the most infamous food poison outbreak in contemporary history." The majority of the affected were under 10 years old. Four children died and 178 others were left with permanent injury including kidney and brain damage.
Food defense is the protection of food products from intentional contamination or adulteration by biological, chemical, physical, or radiological agents introduced for the purpose of causing harm. It addresses additional concerns including physical, personnel and operational security.
American Public Health Association v. Butz, 511 F.2d 331 was a United States Court of Appeals for the District of Columbia Circuit case argued on January 22, 1974, and decided on December 19, 1974.
Salmonellosis annually causes, per CDC estimation, about 1.2 million illnesses, 23,000 hospitalizations, and 450 deaths in the United States every year.
The 2018 American salmonella outbreak was an American foodborne disaster that started in Iowa, spreading to 7 other states, sickening as many as 265 people, killing one, with 94 hospitalized. Ready-to-eat chicken salad was produced by Iowa-based Triple T Specialty Meats Inc. between January 2 and February 7 for distribution in Fareway grocery stores. Salad was sold in containers of various weights at Fareway stores deli from January 4 to February 9. Total of approximately 20 630 pounds of chicken were deemed contaminated with Salmonella Typhimurium at the time of recall on February 21.
Antibiotic use in the United States poultry farming industry is the controversial prophylactic use of antibiotics in the country's poultry farming industry. It differs from the common practice in Europe, where antibiotics for growth promotion were disallowed in the 1950s.