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Blog Posts: Meat

July 11th, 2014

Six Books Our Staff are Reading This Summer

By Elizabeth Walek

Nothing beats lounging by the pool with a really great book! Summer is a perfect time to get caught up on reading that you’ve been putting off for weeks. Plus, books are a great way to learn more about the issues Food & Water Watch handles every day. I asked around our offices to find out which socially, politically and environmentally conscious books our staff love lately. Check out our top picks, and share your own summer reading recommendations in the comments!

Read the full article…

June 10th, 2014

Why the Federal Government Should Block the Tyson-Hillshire Merger

By Patrick Woodall meat aisle in grocery store

After several weeks of musical merger chairs, the dust finally settled this weekend leaving Tyson Foods the winner in a bidding war for Hillshire Brands. The nation’s biggest meat and poultry company offered one billion dollars more than it offered a week and a half ago and the deal is now worth about $8.5 billion. The other bidder, Pilgrim’s Pride, withdrew its bid, and the original deal for Hillshire to buy food manufacturer Pinnacle Foods will be scrubbed to pave the way for the Tyson takeover after Hillshire pays Pinnacle a $163 million “breakup” feeRead the full article…

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June 4th, 2014

Can Factory Farms Make YOU Sick?

By Briana Kerensky

It’s really easy to believe that factory farms aren’t your problem. If you don’t eat meat, limit yourself to only local and organic meat, or live in a city, it can be tough to draw a connection between yourself and a factory farm. But with the rise in antibiotic-resistant infections, they’re quickly becoming everyone’s problem.

Follow Food & Water Watch’s flowchart and find out: can factory farms make you sick? Click the image below to get started.

When you’re done, take action: Tell Congress to save antibiotics for medicine, NOT factory farms.

Click to go to the full flowchart.

 

May 30th, 2014

Hostile Takeover with a Twist

By Patrick Woodall meat aisle in grocery store

Remember those halcyon days when you could grill a Ball Park hot dog or Jimmy Dean sausage without a Wall Street bidding war breaking out? You know, at last Monday’s Memorial Day picnic? 

Because on Tuesday, Brazilian protein powerhouse JBS/Pilgrims Pride made a $6.4 billion dollar unsolicited, hostile takeover offer for Hillshire Farm, which owns the iconic processed pork brands. Then on Thursday, Tyson Foods upped the ante with a $6.8 billion bid for Hillshire. This battle aims to put a sausage link in the food chain of one of America’s top two meat companies. Both of these offers would require Hillshire to abandon its attempt to buy Pinnacle Foods. Read the full article…

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May 8th, 2014

Collaboration or Obfuscation?

By Tony Corbo 

Recently, USDA’s Food Safety and Inspection Service (FSIS) and the Animal and Plant Health Inspection Service (APHIS) agreed to share information during the investigation of foodborne illness outbreaks. A laudable effort since animal diseases and pathogens that lurk in animal husbandry can often lead to human foodborne illnesses. But this recent announcement is clouded by the revelation that FSIS may have deliberately delayed the release of an audit report that revealed some serious shortcomings in the Brazilian meat safety system. Had that report been publicly released on the date that it had been transmitted to the Brazilian government, on April 16, 2014, it would have provided valuable information for a proposed APHIS rule to green light the importation of fresh beef products from Brazil. The comment period on the APHIS proposed rule ended on April 22, 2014. Apparently, the FSIS audit report was only recently posted on its website and was made public as a result of a Freedom of Information Act (FOIA) request filed by the National Cattlemen’s Beef Association (NCBA). Read the full article…

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May 2nd, 2014

FSIS’s Fantasy World

By Tony Corbo

Today, officials from USDA’s Food Safety and Inspection Service (FSIS) are escorting a congressional delegation on tours of two poultry slaughter and processing facilities in the Shenandoah Valley of Virginia operated by George’s Chicken. One is a plant that receives traditional inspection with a full complement of USDA inspectors and the other is a pilot plant that has been using the privatized inspection scheme called the HACCP-based Inspection Models Project (HIMP) where most of the on-line inspection is turned over to company employees called “sorters” to perform.

FSIS has conducted dozens of tours at these two plants over the past decade. Over the years, we have heard about the extraordinary preparations that the George’s HIMP plant in Edinburg, Virginia, has undertaken for these “VIP” tours. Walls have been scrubbed and even repainted; floors have been meticulously cleaned; and the speeds of the slaughter lines have been reduced. Two years ago, I told FSIS agency officials that they have conducted so many tours of that plant that the new AAA Tour Book for Virginia lists the Edinburg HIMP plant as a must-see tourist stop and to call FSIS to make reservations for the “Fantasy Tour.”

In the past, whenever congressional staff, White House staff, consumer representatives or other prospective visitors have asked to visit HIMP plants other than the George’s Edinburg facility, FSIS has balked. That is because the Edinburg plant is the so-called “showcase” plant.  It is immaculate on the inside, FSIS can easily control the tour, access to the plant workers is restricted, and no one is able to look at the plant’s production or safety records to see if there have been any past problems. Fortunately, when the Government Accountability Office (GAO) conducted its study of HIMP in 2013, the analysts were able to visit several different HIMP plants and concluded that since the data was lacking, FSIS could not make the claims that poultry slaughtered in HIMP plants was safer than the product that received traditional inspection. Read the full article…

April 2nd, 2014

If the Drug Companies Love FDA’s New Guidance, Should We?

drug take-back day

Photo by Tom Varco used with permission.

By Sarah Borron

Last week, FDA pronounced success in its voluntary Guidance to Industry #213 on the use of medically important antibiotics in feed for livestock. Every company but one that makes these drugs said they would participate, covering over 99 percent of the affected drugs. If the companies stick to their word, it means that in three years, medically important antibiotics should 1) no longer be used for growth promotion and 2) be used only under the oversight of a veterinarian. Both of these are long overdue first steps, but they still are not enough to stop the overuse of these critically important drugs for a couple of key reasons:

1) Overlap of Use: Giving healthy animals low doses of medically important antibiotics to make them grow faster is a really wasteful use of antibiotics. This practice promotes the development and spread of antibiotic-resistant bacteria, putting profits ahead of public health. It’s high time this practice ended. Unfortunately, the same practice of giving healthy animals low doses of antibiotics can be done in the name of “disease prevention,” which is still allowed under the new FDA guidance. Of the drugs losing their approvals for growth promotion uses, 63 percent are still approved for disease prevention. So, producers aren’t necessarily going to lose the growth promoting benefit of many of the drugs, even if the purpose of using them is disease prevention. Only 11 percent of the drugs will fully discontinue nontherapeutic uses, any use for a purpose other than disease treatment.

2) Strength of Veterinary Oversight: But what about the veterinary oversight? Won’t that stop the use of antibiotics for routine disease prevention? That’s still unclear. FDA just accepted public comments on the Veterinary Feed Directive (VFD), which spells out the rules around veterinarians approving the use of antibiotics in feed. It’s possible that the rules will be written in such a way that veterinarian approval can carry on for months at time or for multiple herds or flocks of animals, possibly without the veterinarian ever visiting the farm. There is also an important issue that the FDA needs to address, the shortage of veterinarians in rural areas. While we want to ensure that lack of access to veterinarians for small farms is addressed, we do have to make sure that this doesn’t become an excuse for allowing injudicious uses of antibiotics to continue on large operations.

In three years, we’ll have a better sense of whether FDA’s initiative offers more shine than substance in changing practices. Regardless, to save antibiotics, we.need Congress to pass a complete ban on nontherapeutic uses of antibiotic use in livestock, and you can help us by asking for your members of Congress to support this important legislation here.

March 11th, 2014

How the FDA’s Voluntary Guidance Fails to Curb Antibiotic Misuse in Livestock

Click to enlarge.

By Sarah Borron

Last December, FDA released voluntary guidance to industry (GFI #213) that would limit certain nontherapeutic uses of what the agency deems “medically important” antibiotics in livestock and put those drugs under the guidance of a veterinarian. Currently, many antibiotics are available for livestock producers to use for nontherapeutic reasons and without veterinary oversight. FDA’s action to curb these uses is long overdue.

But that guidance comes with a catch. It only limits the use of medically important antibiotics for promoting faster growth in livestock. Giving livestock low doses of antibiotics necessary to treat human illnesses to make the animals grow faster – all the while creating antibiotic-resistant bacteria in those livestock – is a pretty terrible use of an important resource. However, the FDA guidance still permits low doses of antibiotics to be given to healthy animals as disease prevention. Whether for growth promotion or disease prevention, the result is the same: this practice is creating more bacteria resistant to antibiotics that we need to protect human health.

Food &Water Watch analyzed FDA’s list of over 400 antibiotic drug products affected by GFI #213 to find out just how much overlap exists between growth promotion uses, which are being limited, and prevention uses, which remain unchecked. Each drug has a list of “label indications,” or reasons the drug can be used in certain conditions. Using FDA’s search function and also reading each label, we identified overlapping indications that demonstrate significant loopholes in GFI #213. Read the full article…

March 5th, 2014

Wenonah Hauter Challenges You to Take Action on the Filthy Chicken Rule

Recognize These Folks? They Are Funny. Factory Farms Are Not

Food & Water Watch Executive Director and Foodopoly author Wenonah Hauter recently attended her third TEDxManhattan to, as she put it, “talk about one of the bummers.” Again.

The U.S. Department of Agriculture is pushing the “Modernization of Poultry Slaughter Inspection” rule, more aptly called the “Filthy Chicken Rule,” and it impacts all of us, whether we eat chicken or not. If implemented, it would:

Read the full article…

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January 24th, 2014

Email Shows USDA Cowering to Industry on Poultry Safety — Again

By Wenonah Hauter

Wenonah Hauter, executive director of Food & Water Watch

Late last week, Food & Water Watch received information that USDA’s Food Safety and Inspection Service (FSIS) was going to permit a trade association — the National Chicken Council —  to collect data in poultry plants to assess the rate of foodborne pathogens in chicken parts. The information came in the form of an e-mail from the Assistant FSIS Administrator for Field Operations Daniel Engeljohn, informing his district managers that he was aware of the effort and gave his full blessing to the project. What was troubling about the e-mail was that it told the district managers that the purpose of the data collection was for the industry to develop its own voluntary pathogen performance standards that it was going to enforce on poultry processing plants. It went on to say that FSIS inspection personnel assigned to the plants were not to interfere with the National Chicken Council data collection and that they had no right to look at the data that was collected.

In other words, the poultry industry would create the standards for pathogen levels in chicken parts, and they would only “voluntarily” stick with them. Not only would the industry be able to decide how much salmonella or campylobacter there is on your chicken, but there would be no USDA enforcement of the standard.

Welcome to the latest in privatization of chicken inspections that the industry is pushing, with the USDA’s blessing. Another example is the “Modernization of Poultry Slaughter Inspection,” the proposed plan whose “modern” twist is to turn most poultry inspection over to the very companies that produce our poultry, leaving only one government inspector per plant to inspect over 175 birds per minute — or three birds per second.

This hasn’t happened overnight. The industry has been chipping away at the USDA’s mandate to protect our food system for over a decade. Since the late 1990s, FSIS has established pathogen performance standards on the meat and poultry industry. The standards were supposed to be enforceable, but the agency lost a critical court case in 2000 when the industry successfully challenged their legality because the current meat and poultry inspection laws are silent on pathogen standards. There were a couple of attempts by Congress in the early 2000s to give FSIS authority to set enforceable pathogen performance standards, but they failed. Senator Kirsten Gillibrand (D-NY) recently introduced a bill, S. 1502, The Safe Meat and Poultry Act, that would give FSIS that authority, but that bill has still not received a hearing.

In the meantime, FSIS has continued to set pathogen performance standards, but they are voluntary for the industry. For salmonella, FSIS will post on its website monthly those poultry plants that fail the agency’s testing program. The agency has claimed that its sampling program has shown that the levels of salmonella in whole raw chicken carcasses have been declining in recent years. However, the Centers for Disease Control continues to report that the number of food borne illnesses attributed to salmonella remains stubbornly high.

In 2010, Consumer Reports conducted its own study of food borne pathogens found in chicken parts.  Consumers rarely buy whole chicken carcasses, but they buy chicken parts in packages at the grocery store. It found that 62% of the chicken parts they bought and analyzed tested positive for campylobacter and 14% tested positive for salmonella.  

In response to the Consumer Reports findings, FSIS – to its credit – began a study to assess the levels of pathogens in chicken parts. In 2012, it posted the results of its survey on its website, which found that 26.3% of the chicken parts were contaminated with salmonella and 21.4% were contaminated with campylobacter. Agency officials have indicated that it was their intent to set government pathogen performance standards for chicken parts. In fact, the Salmonella Action Plan released by the agency in December 2013 listed that as one of the activities for FY 2014 Now, we find out that the industry is going to set its own standards that it will enforce.

In December 2013, Consumer Reports released data on a new study on pathogen contamination in chicken parts that found 43% of the chicken breasts sampled were contaminated with campylobacter and 10.8% with salmonella.

In light of the rule proposed by FSIS in January 2012 that would turn over most inspection responsibilities over to the poultry companies to perform themselves, the Engeljohn e-mail seems to indicate that there is a dangerous deregulatory effort underfoot that would take FSIS out of the food safety business altogether. Instead of trying to enhance its ability to regulate food safety standards, this agency seems to be turning the keys over to the industry to police itself. That is not in the interest of public health and it needs to be stopped.

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