09 DEC 2003 New FDA Tests Show Higher Than Expected Mercury
Levels in Tuna
EWG
Analysis
EWG
Tuna Calculator
EWG
News Release
EWG
presentation to advisory panel
EWG's
Legal Challenge
FDA
Food Advisory Committee docs
Related EWG Content
EWG Mercury and
Seafood Issue Page
EWG Study Finds
FDA Out to Lunch on Protecting Women from Mercury in Fish
EWG
Report: Brain Food
U.S.
Mercury Standard Among Worst in World |
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Summary: EWG's Legal Challenge
EWG will use a newly enacted law (the Data Quality Act (DQA) of
2001) to mount a novel legal challenge to the Food and Drug
Administration's (FDA) highly controversial pending "advice" to
consumers about how much tuna and other fish they can safely eat
without risking their health, and in particular the health of
fetuses, infants and young children, from mercury exposure.
The DQA was originally conceived by and enacted on behalf of
industry lobbyists who wanted to create additional barriers to
federal health, labor and environmental officials updating or
changing a range of government standards. The law requires a "sound
science" basis for any new government standard or protection. It
also requires that the new standard meet certain criteria of:
quality, utility, objectivity, transparency and reproducibility of
information. The criteria are based on guidelines in effect at the
relevant agency (in this case FDA) and the White House Office of
Management and Budget (OMB).
EWG will file the challenge the week of December 15, contending
that the FDA is failing to meet the scientific and regulatory
requirements of the Data Quality Act in proposing to tell American
women that it is safe to eat 12 ounces of tuna a week. The advice
was reviewed for public use at a Dec. 10-11 meeting between FDA
officials and members of FDA's Food Advisory Committee.
In fact, the agency's proposed advice to consumers — eat 12
ounces of fish a week — if followed, could result in more women
getting unsafe levels of mercury in their bodies than they currently
do — assuming they have no other exposure to mercury than that from
tuna. Eight percent of American women of childbearing age — about
four million women — have unsafe levels of mercury in their
blood.
Basis of the legal challenge
The advice FDA is proposing to give women fails the Data Quality
Act test in a number of ways:
- It is not useful. If followed, FDA proposed advisory
would actually increase consumption of fish with significant
levels of mercury contamination and cause many more women to go
through pregnancy with unsafe levels of mercury in their blood.
- It is not clear, comprehensive or understandable.
Except for the four fish on its "do not eat" list, the advisory
provides no specific information on how to consume fish in a
fashion that ensures that a woman will not expose her unborn child
to an unsafe dose of mercury throughout pregnancy.
- It is not transparent and reproducible. The agency has
not examined what effect its proposed advice would have on mercury
levels in the general population if it were actually followed. If
its officials have conducted such an analysis, they have not made
it available to the public, making it impossible for anyone to
reproduce the science and risk assessments behind the proposed
advice.
- It is not based on scientifically sound practices.
FDA's consumption advice is based on inadequate testing data and
faulty analyses that lead the agency to recommend eating types of
seafood that are not, in fact, safe to eat in the quantities
recommended.
How the challenge will work
EWG files its challenge with FDA, and the agency must review the
challenged decision based on DQA guidelines of OMB and Department of
Health and Human Services. A successful challenge under Data Quality
Act demands rejection of federal agency guidance or rulings, which
do not meet the basic standards of quality, and correction of the
information to comply with the guidelines.
EWG will proceed through the appropriate agency administrative
channels, if FDA fails to correct the information. EWG will then
file a lawsuit in Federal District Court, if necessary, to require
FDA to produce a scientifically sound advisory. The Data Quality Act
can be used to file a lawsuit where a federal agency has
consistently overruled a challenge internally through all of the
administrative channels. |