{"id":5212,"date":"2014-10-27T11:00:42","date_gmt":"2014-10-27T15:00:42","guid":{"rendered":"http:\/\/circulatingnow.nlm.nih.gov\/?p=5212"},"modified":"2022-11-13T15:24:30","modified_gmt":"2022-11-13T20:24:30","slug":"adulterated-and-misbranded-foods-fda-notices-of-judgment","status":"publish","type":"post","link":"https:\/\/circulatingnow.nlm.nih.gov\/2014\/10\/27\/adulterated-and-misbranded-foods-fda-notices-of-judgment\/","title":{"rendered":"Pure Food: FDA Notices of Judgment"},"content":{"rendered":"

Circulating Now welcomes guest blogger<\/em> Dr. Suzanne Junod, a historian in the FDA History Office<\/a>. In celebration of the completion of NLM\u2019s digital archive of court case summaries published as the Food and Drugs Act Notices of Judgment<\/a>, Dr. Junod offers a brief history of U.S. food and drug regulation and a use case for the areas of research the collection offers.<\/em><\/p>\n

\"Theodore<\/a>
Theodore Roosevelt, ca. 1915
Photography by Pach Brothers<\/em>
Courtesy Library of Congress<\/em><\/a><\/figcaption><\/figure>\n

The 1906 Pure Food and Drugs Act is generally viewed by historians as a signature achievement of the Progressive Era in American history and this founding statute established what would become today\u2019s Food and Drug Administration. From the time a statute was first proposed in 1880 until the day on which Theodore Roosevelt signed it into law\u2014June 30, 1906\u2014it had taken 100 bills and 27 years to enact a federal law to protect consumers from adulterated and misbranded foods and drugs moving across state lines. Some states had protective statutes, and some worked better than others, but increasingly states themselves supported federal protection from spurious, mislabeled, and substandard products. True or not, for example, supporters of the new federal law claimed that there was more ordinary corn syrup claiming to be \u201cPure Vermont Maple Syrup\u201d shipped from Iowa each year, than Vermont had produced of the genuine article since the settlers arrived. Without a federal law, Vermont was nearly helpless to stop shipments of the counterfeit product. With it, they could literally \u201cmake a federal case\u201d out of it.<\/p>\n

Making a federal case, however, depended on careful documentation and detailed records, something at which the Bureau of Chemistry<\/a>, the predecessor of the Food and Drug Administration, excelled.\u00a0\u00a0 These early federal records were required to be held \u201cuntil repeal of the enabling legislation.\u201d In 1938, Congress did just that.\u00a0\u00a0 It repealed the 1906 statute and replaced it with a new federal food and drugs statute that is still the law of the land today: the 1938 Food, Drug, and Cosmetic Act. As a result, many of the earliest Bureau of Chemistry records were destroyed. Years later, however, my colleague, John Swann, and I in the FDA History Office discovered a treasure trove of these records: the case seizure files documenting all enforcement actions under the 1906 statute. These records were later transferred to NLM\u2019s History of Medicine collections and inspired the multi-year collaboration to digitize the published notices of judgment, the final outcomes of the \u2018federal cases.\u2019 This collection offers insight into U.S. legal and governmental history, as well as the evolution of clinical trial science and the social impact of medicine on health. The legal history of some of our best-known consumer items of today, such as Kellogg\u2019s Corn Flakes, can be traced in the collection. Product packaging and labeling, including the cereal packaging below, are commonly found in the prosecutorial evidence files of the collection.<\/p>\n