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1 | HOUSE RESOLUTION
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2 | WHEREAS, Bisphenol A (BPA) is found in many consumer | ||||||
3 | products, such as baby bottles and other reusable containers | ||||||
4 | made from polycarbonate plastic and in the epoxy resin coating | ||||||
5 | used in most food and beverage cans, including canned infant | ||||||
6 | formula; and
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7 | WHEREAS, Upon the request of the Commissioner of the United | ||||||
8 | State Food and Drug Administration (FDA), the FDA formed an | ||||||
9 | agency-wide BPA task force to facilitate cross-agency review | ||||||
10 | and evaluation of current research and new information on BPA | ||||||
11 | for all FDA regulated products and to make recommendations to | ||||||
12 | the Commissioner regarding actions the FDA should take next | ||||||
13 | regarding BPA; and
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14 | WHEREAS, As part of its evaluation, the task force has | ||||||
15 | reviewed the concerns presented in the National Toxicology | ||||||
16 | Program Brief published in September 2008 by the National | ||||||
17 | Institutes of Health and the concerns presented in the Canadian | ||||||
18 | risk assessment released in October 2008; and
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19 | WHEREAS, The FDA has considered the research and positions | ||||||
20 | of other transnational food safety organizations, including | ||||||
21 | the 2 risk assessments for BPA conducted by the European Food | ||||||
22 | Safety Authority's Scientific Panel on Food Additives, |
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1 | Flavourings, Processing Aids and Materials in Contact with Food | ||||||
2 | and the Japanese National Institute of Advanced Industrial | ||||||
3 | Science and Technology; each of these documents considered the | ||||||
4 | question of a possible low-dose effect and concluded that no | ||||||
5 | current health risk exists for BPA at the current exposure | ||||||
6 | level; and
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7 | WHEREAS, The FDA has been reviewing the emerging literature | ||||||
8 | on BPA on a continuous basis; and | ||||||
9 | WHEREAS, In August 2008, the FDA released a draft safety | ||||||
10 | assessment of BPA in food contact products and in October 2008, | ||||||
11 | the FDA Science Board provided recommendations to the FDA to | ||||||
12 | improve the safety assessment; and | ||||||
13 | WHEREAS, The FDA has reported back to the Science Board on | ||||||
14 | February 24, 2009 on the progress they have made to address the | ||||||
15 | Science Board recommendations; and
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16 | WHEREAS, It is altogether fitting and proper and in the | ||||||
17 | public interest for us to urge the United States Food and Drug | ||||||
18 | Administration to expedite their current review of bisphenol A | ||||||
19 | in food containers and baby bottles; therefore, be it
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20 | RESOLVED, BY THE HOUSE OF REPRESENTATIVES OF THE | ||||||
21 | NINETY-SIXTH GENERAL ASSEMBLY OF THE STATE OF ILLINOIS, that we |
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1 | urge the United States Food and Drug Administration to expedite | ||||||
2 | its current review of the safety of bisphenol A in products | ||||||
3 | that contact food and take appropriate action based on its | ||||||
4 | findings; and be it further | ||||||
5 | RESOLVED, That a suitable copy of this resolution be | ||||||
6 | presented to the Commissioner of the United States Food and | ||||||
7 | Drug Administration and each member of the Illinois | ||||||
8 | congressional delegation.
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