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1 | SENATE RESOLUTION
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2 | WHEREAS, Bisphenol A (BPA) is found in many general | ||||||
3 | plastics, such as food and drink packaging, baby bottles, | ||||||
4 | thermoses, and other reusable plastic containers, and is used | ||||||
5 | as an epoxy can liner, coating items such as food cans, | ||||||
6 | bottles, and water supply pipes, and in the production of | ||||||
7 | polycarbonate plastics; and
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8 | WHEREAS, Upon the request of the Commissioner of Food and | ||||||
9 | Drugs, the U.S. Food and Drug Administration (FDA) formed an | ||||||
10 | agency-wide BPA task force to facilitate the cross-agency | ||||||
11 | review of current research and new information on BPA for all | ||||||
12 | FDA regulated products; as a result of this review, the task | ||||||
13 | force will make recommendations to the Commissioner regarding | ||||||
14 | next steps; and
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15 | WHEREAS, Part of this evaluation will include the FDA Task | ||||||
16 | Force reviewing the concerns presented in the National | ||||||
17 | Toxicology Program Draft Brief published on April 14, 2008 by | ||||||
18 | the U.S. National Institutes of Health and the concerns | ||||||
19 | presented in the Canadian draft risk assessment released in | ||||||
20 | April 2008; and
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21 | WHEREAS, The FDA has been reviewing the emerging literature | ||||||
22 | on BPA on a continuous basis and has recently completed a |
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1 | review of the available biological fate data and 2 recently | ||||||
2 | completed rodent multigeneration reproductive studies, and | ||||||
3 | these studies did not indicate a safety concern for BPA at | ||||||
4 | current exposure levels; in addition, the FDA is conducting a | ||||||
5 | review of the data on neural and behavioral effects of BPA | ||||||
6 | exposure; and
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7 | WHEREAS, The FDA will consider the research and positions | ||||||
8 | of other transnational food safety organizations, including | ||||||
9 | the 2 risk assessments for BPA conducted by the European Food | ||||||
10 | Safety Authority Scientific Panel on Food Additives, | ||||||
11 | Flavourings, Processing Aids and Materials in Contact with Food | ||||||
12 | and the Japanese National Institute of Advanced Industrial | ||||||
13 | Science and Technology; each of these documents considered the | ||||||
14 | question of a possible low-dose effect and concluded that no | ||||||
15 | current health risk exists for BPA at the current exposure | ||||||
16 | level; and
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17 | WHEREAS, In January 2008, the United States House of | ||||||
18 | Representatives Committee on Energy and Commerce began | ||||||
19 | reviewing the use of bisphenol A in products intended for use | ||||||
20 | by infants and children; and
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21 | WHEREAS, It is altogether fitting and proper and in the | ||||||
22 | public interest for this Senate to urge the United States Food | ||||||
23 | and Drug Administration to expedite their current review of |
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1 | bisphenol A in food containers, toys, and baby bottles; | ||||||
2 | therefore, be it
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3 | RESOLVED, BY THE SENATE OF THE NINETY-FIFTH GENERAL | ||||||
4 | ASSEMBLY OF THE STATE OF ILLINOIS, that we urge the United | ||||||
5 | States Food and Drug Administration to expedite their current | ||||||
6 | review of bisphenol A; and be it further
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7 | RESOLVED, That suitable copies of this resolution be | ||||||
8 | delivered to the President and Vice President of the United | ||||||
9 | States, the Commissioner of the United States Food and Drug | ||||||
10 | Administration, and each member of the Illinois congressional | ||||||
11 | delegation.
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