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Writers Articles And Opinions |
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01 September 2010 By Stephen
Lendman
On July 29, 2009, the House
passed HR 2749: Food Safety Enhancement Act of 2009
"To amend the (1938 as amended) Federal Food, Drug,
and Cosmetic Act to improve the safety of food in the
global market, and for other purposes."
An earlier July 2009 article
discussed it, accessed through the following link:
http://sjlendman.blogspot.com/2009/07/hr-2749-agribusiness-empowering-act.html
On March 3, 2009, S. 510: FDA
Food Safety Modernization Act was introduced as the
Senate's version of the House bill. On December 18,
2009, it cleared committee and was placed on the
Senate's Legislative Calendar for consideration. Thus
far not addressed, it likely will be and passed in the
wake of the egg salmonella scare though, like its
companion bill, it's for agribusiness empowerment, not
food safety, used as cover to enhance greater industry
consolidation at the expense of small farmers and
consumers.
Current laws and regulations are
adequate but not enforced, with good reason. Run by
industry officials, the USDA is woefully understaffed,
under-budgeted, and only performs perfunctory
inspections. The FDA operates the same way, fronting
for agribusiness, Big Pharma, and related industries,
not consumer protection.
If House and Senate bills pass,
it will gain new powers and fewer judicial restraints
on its actions. Although some provisions address
improving America's food, the bills' vague and
deceptive language increases the potential for
inappropriate application and enforcement, harming
small farmers and consumers for big business, what's
vital to avoid but less likely given the egg recall.
Now there's a push for corporate
friendly legislation masquerading as pro-consumer, the
way Congress always works. So expect the worst, for
sure what Obama supports, stiff-arming his
constituents across the board in deference to
corporate and power interests.
According to the National
Independent Consumers and Farmers Association, S. 510:
"will have the unintended
destructive consequence of eliminating small farms and
consumer access to local food (because it) grants
sweeping powers to the (FDA) and US Dairy Association,
(imposes harmful new regulations, and lets federal)
agents go on to (small) farms, where less than one
half of one percent of food-borne illnesses originate,
(nearly all of it from factory farms) without having
credible evidence that a problem exists, needing only
'reason to believe' in order to quarantine or shut
down a farm."
PPJ Gazette writer Marti Oakley
calls the Senate bill (and by inference the House one)
the "Making America Sick Through Adulteration of Food"
act, saying the nation "is only as successful as its
farmers and ranchers" able to feed the public at all
times. "And by farmers and ranchers I don't mean
industrialized corporate farming for massive profits
while we defile everything in sight," including safe
food because FDA and USDA officials front for
business, not consumers, on their own without
protection.
The Farm-to-Consumer Legal
Defense Fund (FTCLDF) on Food Safety and Congressional
Legislation Not Designed to Protect It
FTCLDF (the Fund) represents
family farmers' right "to provide processed and
unprocessed farm foods directly to consumers," and
their right to buy them from family farms. It also
protects small farms "from harassment by federal,
state, and local government interference with food
production and on-farm food processing."
The Fund opposes the House and
Senate bills, saying they threaten "to leave small
farmers and local producers unable to afford the cost
of complying with legislative requirements." In
addition, the FDA will be more greatly empowered to
help agribusiness and harm local farming and
consumers. Besides, "neither bill would improve food
safety" because that's not their purpose.
Their anti-consumer provisions
will empower bigness, increase imported food, create
new safety concerns, and restrict the ability of
Americans to get food choices they want from sources
they prefer.
Unmentioned in the House bill, S.
510 references the Department of Homeland Security
(DHS) 22 times, especially in Section 108(a)(1),
calling for the Health and Human Services (HHS) and
Agriculture secretaries to coordinate with HHS to
prepare and submit to Congress the "National
Agriculture and Food Defense Strategy."
Sounding more like preparing for
war than food safety, Section 108(5) requires the
strategy be consistent with the National Incident
Management System, the National Response Framework,
the National Infrastructure Protection Plan, and the
National Preparedness Goals - programs created by
presidential Executive Orders and National Security
Directives, (not acts of Congress) to help big, not
small farmers or consumers.
For example, over "terrorism"
hysteria, the 2004 Homeland Security Presidential
Directive (HSPD) 9 designated DHS "responsible for
coordinating the overall national effort" to protect
America's food system, its Secretary "the principal
federal official to lead, integrate, and coordinate
federal, state, local and private sector elements."
Of concern is HHS' role in "food
defense and critical infrastructure protection." In
2007, its Office of Inspector General suggested why,
based solely on three minor incidents, including:
-- in 1984, an Oregon religious
cult poisoning 10 salad bars causing 751 illnesses;
-- in 1996, a Texas hospital
employee tainting the facility's snacks causing 12
illnesses; and
-- in 2003, a Michigan
supermarket employee infecting 200 pounds of beef
causing 92 illnesses, hardly reasons to wage war on
bad food and call out the Marines.
Yet, according to the Centers for
Disease Control and Prevention (CDC), unintentional
food contamination (raising no eyebrows) cause 76
million food-related illnesses annually.
In addition, the 2007 OIG report
explained that:
-- DHS consolidated 22
preexisting agencies and organizations, all unrelated
to food;
-- the sector's size and
complexity poses vexing challenges, compounded by new
DHS food sector obligations compromised by
incompatible internal documents;
-- the agency has "no major
organizational entity (focused) exclusively or even
largely" on food;
-- no DHS official has overall
food responsibility; and
-- other inconsistencies in its
new mandate, assuring snafus doing more harm than
good.
"A more effective way to protect
our food supply is to create" more localized diversity
nationwide, not greater concentration and a war
against food terrorists.
Yet passing legislation with
Section 108 "would be a major step toward" putting the
nation's food system "on a permanent crisis-mode
footing." Instead of federalizing supply and enhancing
agribusiness power, our best food defense "is to
promote the decentralization of food production,
encouraging local communities" to be as
self-sustaining as possible.
In other words, promote small and
local, not big and global, a sure formula for higher
prices, less variety, weaker consumer protections, and
greater likelihood for tainted products because
industry officials run the FDA and USDA before
recycling back into high-paying corporate jobs. In
both capacities, their job is maximizing profits, not
food safety.
The Movement of
Food
Information from the
above-referenced link details concerns with HR 2749,
including:
Establishing enforcement
authority under Section 133 to restrict the movement
of food, giving unelected officials power to shut down
food movement in a state by quarantine without court
order.
Criminal and
Civil Penalties
Under Sections 134 and 135,
criminal or civil penalties are imposed against anyone
alleged to knowingly introduce or deliver adulterated
or misbranded food through interstate commerce, the
penalty being 10 years in prison.
Under current law, it's one year
or three in cases of willfully defrauding or
misleading. Civil penalties are also stiffer, as high
as $7,500,000 (up from a maximum $250,000) for a
corporate offender (including small ones), each day in
violation considered a separate offense. Even delays
in complying with registration requirements carry
substantial fines.
As a result, these provisions let
the FDA "harass and bankrupt small farmers and local
producers" to help large ones, the reason for their
inclusion, corporate lawyers, of course, writing these
bills, the same procedure for all congressional
legislation, including healthcare and financial
reform, to protect their bottom-line concerns.
HACCP Plans
HR 2749, Section 102 and S. 510,
Section 103 require registered facilities to have
written Hazard Analysis Critical Control Points (HACCP)
plans, prepared by:
-- conducting a hazard analysis;
-- identifying, implementing, and
monitoring effective preventive controls;
-- instituting corrective actions
if needed;
-- providing verification;
-- maintaining proper records;
and
-- reanalyzing for hazards as
needed.
Evaluating HACCP based on past
meat industry experiences shows that corporate
slaughterhouses and processing plants "operate in the
relative absence of USDA inspections," in many cases
none at all or personnel occasionally showing up but
not doing their job.
Yet, the USDA's Food and Safety
Inspection Service (FSIS) web site states that
"Slaughter facilities cannot operate if FSIS
inspection personnel are not present (and) Only
Federally inspected establishments can produce
products that are destined to enter commerce."
In contrast, small plants are
harassed, burdened with extra paper work, and targeted
with more enforcement actions - many, as a result,
driven out of business; from 2000 - 2005 alone, a
21.9% decline in processing plants and 19% for
slaughterhouses.
Food
Traceability
Under HR 2749, Section 107, the
HHS Secretary is mandated to establish a domestic and
imported food tracing system, using "identif(ied)
technologies and methodologies" burdensome to small
producers. It's to let the Secretary "identify each
person who grows, produces, manufactures, processes,
packs, transports, holds or sell such food" in the
shortest practicable time but "no longer than two
business days."
Exempted is food produced on
owner, operator or agent in charge farms, selling
directly to consumers, restaurants or stores. Records
must still be kept at least six months, and farmers
selling to other ones or wholesalers are subject to
traceability requirements.
The provision is about "further
integrating the American food system into the global
market" to help agribusiness and harm small
competitors. Instead of greater globalization, US
policy should promote local self-sufficiency, a notion
not in Congress' or regulatory agencies' vocabulary in
deference to the corporate interests they serve.
The FDA and USDA (like all
federal agencies) don't "protect the health of the
American people but rather" the profits of industry
producers.
Produce Safety
Standards
HR 2749, Section 104 and S. 510,
Section 105 deal with standards for produce safety to
minimize health risks, from growing to transporting
and storing it. Even local roadside stands and
farmers' markets would be subject to national safety
standards, including record keeping, under FDA
jurisdiction. Of concern is the cost burden on many,
perhaps great enough shut them down, the whole idea
behind these provisions.
Survey Results
Reveal Other Problems
A 2008 Resource Conservation
District of Monterey County, CA survey of 600
irrigated raw crop growers found 8% had their crops
rejected for reasons including:
-- deer intrusion;
-- "potential frog habitat;"
-- the "presence of frogs and
tadpoles in creek;"
-- planted crops "near trees
needed a buffer of 100 to 150 feet;" and
-- "deer tracks near" one
farmer's field.
Overall, so-called good
agricultural practices (GAPs) are extremely burdensome
to small producers, in many cases driving them out of
business.
Codex Alimentarius (CA) Provision
in S. 510
An earlier article explained
Codex's threat, accessed through the following link:
http://sjlendman.blogspot.com/2009/08/codex-alimentarius-threatens-human.html
Ostensibly created "to develop
food standards, guidelines" and related "codes of
practice," CA, under
World Trade Organization (WTO)
rules, is corporate controlled. It lets global food,
pharmaceutical, and banking giants, in league with
complicit UN and government agencies, promote GMO
foods and drugs, not healthy natural ones. In
addition, it will restrict or prohibit vitamin and
dietary supplements, except ones they control. Also
processed organic foods will be tainted by irradiation
and harmful synthetic additives or ingredients.
If CA's standards and guidelines
are adopted, binding one-size fits all global rules
will be established, overriding sovereign national
laws and safe practices. GMO foods and drugs will
proliferate. Labeling will be banned. Food and drug
giants will decide what will and won't be sold and at
what price. Governments will have no power to
countermand them, and everyone's health will be
jeopardized.
S. 510, Section 306, covers the
capacity of governments with respect to food. Its
subsection (5) recommends bilateral and multilateral
arrangements and agreements, a giant leap toward
implementing CA, what's been ongoing incrementally for
years, the Obama administration on board fast-tracking
it.
On June 10, 2010, a White House
press release announced "Executive Order -
Establishing the National Prevention, Health
Promotion, and Public Health Council," a stealth
CA-endorsing measure about profits, not public
welfare.
Under a de facto CA council, its
"Section 6(g) contains specific plans to ensure that
all prevention programs outside the Department of
Health and Human Services are based on
(industry-crafted) science-based guidelines (said to
have been) developed by the Centers for Disease
Control and Prevention under subsection (d) of this
section."
In other words, all non-corporate
controlled good health, disease-preventing products
and supplements will be banned under full CA
implementation, what's coming unless stopped, what S.
510 tries to legislate, what Barack Obama will sign
into law if successful.
Final Comments
House and Senate bills "represent
landmark legislation that will significantly increase
the federal government's power to regulate intrastate
commerce while hurting (America's) ability to produce
safe food" and achieve local sustainability. Small
farms and producers will be most harmed, the sector
"producing the safest most nutritious food," thus
benefitting agribusiness and importers, those most
responsible for food safety problems.
Rather than declaring war on food
terrorism, Congress should decentralize food
production, processing and distribution, assuring
safer, cheaper, lower priced products. Instead it's
pushing the opposite.
Greater than ever FDA empowerment
will be counterproductive and harmful, its record
tainted by industry control, promoting hazardous to
health GMO foods and unsafe industry practices like
concentrated animal feeding operations (CAFOs), "the
antithesis of food safety," by an agency destructive
to small farmers, local producers and consumers.
Passing S. 510 and reconciling it
with HR 2749 will jeopardize food safety and make it
harder to buy products consumers want from sources
they prefer. Defeating S. 510 is thus crucial, now at
risk by the egg salmonella scare, a large hurtle
essential to overcome.
Stephen Lendman lives in
Chicago and can be reached at lendmanstephen@sbcglobal.net.
Also visit his blog site at sjlendman.blogspot.com and
listen to cutting-edge discussions with distinguished
guests on the Progressive Radio News Hour on the
Progressive Radio Network Thursdays at 10AM US Central
time and Saturdays and Sundays at noon. All programs
are archived for easy listening.
http://www.progressiveradionetwork.com/the-progressive-news-hour/.
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