Bill Text: MN HF3051 | 2011-2012 | 87th Legislature | Introduced


Bill Title: Genetically engineered food regulated.

Spectrum: Partisan Bill (Democrat 1-0)

Status: (Introduced - Dead) 2012-05-09 - Introduction and first reading, referred to Agriculture and Rural Development Policy and Finance [HF3051 Detail]

Download: Minnesota-2011-HF3051-Introduced.html

1.1A bill for an act
1.2relating to food safety; regulating genetically engineered food; authorizing
1.3rulemaking; requiring a report;proposing coding for new law in Minnesota
1.4Statutes, chapter 31.
1.5BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:

1.6    Section 1. [31.98] DEFINITIONS.
1.7    Subdivision 1. Applicability. For the purposes of sections 31.98 to 31.982, the
1.8following terms have the meanings given.
1.9    Subd. 2. Cultivated commercially. "Cultivated commercially" means grown or
1.10raised by a person in the course of the person's business or trade and sold within the
1.11United States.
1.12    Subd. 3. Enzyme. "Enzyme" means a protein that catalyzes chemical reactions of
1.13other substances without being destroyed or altered upon completion of such reactions.
1.14    Subd. 4. Genetically engineered. "Genetically engineered" means any food that
1.15is produced from an organism or organisms in which the genetic material was modified
1.16through the application of: (1) in vitro nucleic acid techniques, including recombinant
1.17deoxyribonucleic acid techniques and the direct injection of nucleic acid into cells or
1.18organelles; or (2) fusion of cells, including protoplast fusion, or hybridization techniques
1.19that overcome natural physiological, reproductive, or recombination barriers, where the
1.20donor cells or protoplasts do not fall within the same taxonomic family, in a way that does
1.21not occur by natural multiplication or natural recombination.
1.22    Subd. 5. Organism. "Organism" means any biological entity capable of replication,
1.23reproduction, or transferring genetic material.
2.1    Subd. 6. In vitro nucleic acid techniques. "In vitro nucleic acid techniques"
2.2means techniques, including, but not limited to, recombinant deoxyribonucleic acid
2.3or ribonucleic acid techniques, that use vector systems and techniques involving the
2.4direct introduction into the organisms of hereditary materials prepared outside the
2.5organisms such as microinjection, macroinjection, chemoporation, electroporation,
2.6microencapsulation, and liposome fusion.
2.7    Subd. 7. Processed food. "Processed food" means any food other than a
2.8raw agricultural commodity and includes any food produced from a raw agricultural
2.9commodity that was processed through canning, smoking, pressing, cooking, freezing,
2.10dehydration, fermentation, or milling.
2.11    Subd. 8. Processing aid. "Processing aid" means: (1) any substance that is added to
2.12a food during the processing of such food but that is removed in some manner from the
2.13food before the food is packaged in a finished form; (2) any substance that is added to a
2.14food during processing that is converted into constituents normally present in the food and
2.15that does not significantly increase the amount of the constituents naturally found in the
2.16food; or (3) any substance that is added to a food for its technical or functional effect in
2.17the processing but that is present in the finished food at insignificant levels and that does
2.18not have any technical or functional effect in the finished food.

2.19    Sec. 2. [31.981] GENETICALLY ENGINEERED FOOD.
2.20(a) On and after July 1, 2014, any food offered for retail sale in this state shall be
2.21deemed misbranded if such food is, or may have been, entirely or partially produced with
2.22genetic engineering and such fact is not disclosed, as follows:
2.23(1) in the case of a raw agricultural commodity, on the package offered for retail
2.24sale, with the clear and conspicuous words "Genetically Engineered" on the front of the
2.25package of such commodity, or in the case of any such commodity that is not separately
2.26packaged or labeled, on a label that appears on the retail store shelf or bin in which such
2.27commodity is displayed for sale; and
2.28(2) in the case of any processed food, in clear and conspicuous language on the front
2.29or back of the package of such food, with the words "Partially Produced with Genetic
2.30Engineering" or "May be Partially Produced with Genetic Engineering."
2.31(b) Nothing in paragraph (a) shall be construed to require either the listing or
2.32identification of any ingredient or ingredients that were genetically engineered, nor that
2.33the term "genetically engineered" be placed immediately preceding any common name
2.34or primary product descriptor of a food.
2.35(c) The requirements of paragraph (a) do not apply to any of the following:
3.1(1) food consisting entirely of, or derived entirely from, an animal that was not
3.2genetically engineered, regardless of whether such animal was fed or injected with any
3.3genetically engineered food or any drug that was produced through means of genetic
3.4engineering;
3.5(2) a raw agricultural commodity or food derived from such commodity that was
3.6raised or produced without the knowing and intentional use of genetically engineered
3.7seed or food, provided any person required to comply with the provisions of this section
3.8obtains a sworn statement from the person providing such commodity or food that such
3.9commodity or food: (i) was not knowingly or intentionally genetically engineered; and
3.10(ii) has been segregated from, and was not knowingly or intentionally commingled with,
3.11food that may have been genetically engineered at any time. In providing such a sworn
3.12statement, any person may rely on a sworn statement from the person's own supplier
3.13that contains such an affirmation;
3.14(3) any processed food that would be subject to the provisions of this section solely
3.15because it includes one or more genetically engineered processing aids or enzymes;
3.16(4) any alcoholic beverage;
3.17(5) until July 1, 2019, any processed food that would be subject to the provisions
3.18of this section solely because such processed food includes one or more genetically
3.19engineered ingredients, provided: (i) no single such ingredient accounts for more than
3.20one-half of one percent of the total weight of such processed food; and (ii) such processed
3.21food does not contain more than ten such ingredients;
3.22(6) food that an independent organization determines was not knowingly and
3.23intentionally produced from or commingled with genetically engineered seed or genetically
3.24engineered food, provided such determination is made pursuant to a sampling and testing
3.25procedure approved in rules adopted by the commissioner. No sampling procedure shall be
3.26approved by the commissioner under this section unless such sampling is: (i) performed
3.27according to a statistically valid sampling plan consistent with principles recommended
3.28by internationally recognized sources such as the International Standards Organization
3.29(ISO) and the Grain and Feed Trade Association (GAFTA); (ii) consistent with the most
3.30recent "Guidelines on Performance Criteria and Validation of Methods for Detection,
3.31Identification and Quantification of Specific DNA Sequences and Specific Proteins in
3.32Foods, (CAC/GL 74 (2010))" published by the Codex Alimentarius Commission; and (iii)
3.33not reliant on testing of processed foods in which no DNA is detectable;
3.34(7) food that is lawfully certified to be labeled, marketed, and offered for sale as
3.35organic pursuant to the federal Organic Food Products Act of 1990 and the regulations
3.36promulgated by the United States Department of Agriculture;
4.1(8) food that is not packaged for retail sale and that either is a processed food
4.2prepared and intended for immediate human consumption or is served, sold, or otherwise
4.3provided in any restaurant or other food facility that is primarily engaged in the sale of
4.4food prepared and intended for immediate human consumption; and
4.5(9) medical food.
4.6(d) The commissioner, in consultation with the commissioner of health, may adopt
4.7rules necessary for the implementation and enforcement of the provisions of this section.
4.8(e) Any person may bring an action in district court to enforce the provisions of this
4.9section and the court shall have jurisdiction upon hearing and for cause shown to grant a
4.10temporary or permanent injunction restraining any person from violating any provision
4.11of this section. In addition to any injunctive relief provided, the court may award to the
4.12person bringing the action reasonable attorney fees and all reasonable costs incurred in
4.13the investigation and prosecution of such action, as determined by the court. Nothing in
4.14this paragraph shall be construed to limit or alter the powers of the commissioner to bring
4.15an action to enforce this section.

4.16    Sec. 3. [31.982] BEST PRACTICES.
4.17The commissioner shall adopt rules that establish best practices for farmers who
4.18cultivate commercially any genetically engineered crop. Such regulations shall require the
4.19implementation of practices by such farmers to: (1) eliminate or minimize the degree to
4.20which such genetically engineered crop affects neighboring lands; and (2) minimize the
4.21amount of herbicides used by such farmers to eradicate herbicide-resistant weeds.

4.22    Sec. 4. DISPLAY PREFERENCE.
4.23No later than October 15, 2012, the commissioner of agriculture shall report to
4.24the legislative committees with jurisdiction over agriculture and health on a method
4.25to implement a program to provide preference in the display of food items at retail
4.26establishments for any food item that is voluntarily labeled in such a manner as to indicate
4.27whether such food item is genetically engineered or contains genetically engineered
4.28ingredients.

4.29    Sec. 5. LIST REQUIRED.
4.30No later than October 15, 2012, the commissioner of agriculture, in consultation with
4.31the commissioner of health, shall publish a list on the Department of Agriculture's Web
4.32site that indicates those raw agricultural commodities known to be genetically engineered.
4.33The commissioner shall update such list not less than once every calendar year.

5.1    Sec. 6. PROCUREMENT GUIDELINES.
5.2No later than January 1, 2013, the commissioner of administration shall develop
5.3recommendations for the implementation of state agency procurement guidelines that will
5.4provide a preference for the use and purchase of processed foods and raw agricultural
5.5commodities that are voluntarily labeled to indicate whether such processed foods or raw
5.6agricultural commodities contain genetically engineered ingredients or are genetically
5.7engineered, respectively. The commissioner shall also submit any requisite statutory
5.8or rule changes for the implementation of such recommendations to the legislative
5.9committees with jurisdiction over agriculture, health, and state government finance.
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