I have known of Mike Taylor since shortly after September 29, 1994. As Food Safety News reported in “Looking Back: The Story Behind Banning E. Coli O157:H7,” Taylor took the podium that day in San Francisco at the American Meat Institute’s annual convention to make his first, and arguably most significant, speech as the top food safety official at the U.S. Department of Agriculture. “I am here to talk about change,” began Taylor, who had just become administrator for the USDA’s Food Safety Inspection Service (FSIS), as he looked out over his all-industry audience. “Change in what the public expects when it comes to food safety, change in how we at the FSIS are approaching our job, and change in the demands being placed on all those who produce, process and market meat and poultry for American consumers.” Taylor explained his belief that the meat industry had an opportunity to move beyond the politics of food safety and find real solutions on the heels of the massive Jack in the Box E. coli O157:H7 outbreak in the Pacific Northwest that had happened a year before. And then, Taylor uttered a few lines the industry may not have wanted to hear:

In one critical respect, our inspection program at FSIS does not currently meet the public expectation. There is a gap in our system. The fact is we do not deal directly enough and scientifically enough with the microbial pathogens that can make people sick.

To clarify an important legal point, we consider raw ground beef that is contaminated with E. coli O157:H7 to be adulterated within the meaning of the Federal Meat Inspection Act.

We are prepared to use the Act’s enforcement tools, as necessary, to exclude adulterated products from commerce.

And with that the world changed. This seemingly simple change – calling E. coli O157:H7 an adulterant – has over the last 20 years saved countless children from kidney failure and death. In the long run it has also saved the beef industry millions of dollars – dollars that would have gone into my pocket and the pockets of clients sickened by that deadly bacterium. And that has been a very good thing. Over the last decades I have bumped into Mike at food safety conferences around the world, as he ushered in HACCP in the meat industry,  as he worked on food safety in academia and as he performs his current food safety role at FDA – forcing the industry to think hard about how to prevent another Jack in the Box. During the run-up to the passage of the Food Safety Modernization Act (FSMA) in 2010, I watched as he deftly helped consumers and industry form partnerships to press for the most comprehensive changes in FDA rules in too many decades. And during the last few years I have watched quietly as a few groups raised questions about his integrity, including a petition to President Obama to fire him. Last Friday I flew from Seattle to spend two hours of Saturday in Boston participating in a panel before some 75 journalists at a session of the annual meeting of the Association of Health Care Journalists. Along with Mike Taylor and Will Daniels (food safety leader at Earthbound Farms), we discussed why foodborne illness persists as a challenging problem and what consumers, government and industry are doing to prevent it. Each of us had about 20 minutes each to speak. The plan then was to open it up for questions. One of the first questions posed to Mike was not about E. coli O157:H7 or how with a limited budget was the FDA trying to implement FSMA. The first question was about Mike’s “Monsanto baggage,” specifically whether his past role working on biotechnology-related matters for Monsanto, created a conflict of interest for his current role at FDA as Deputy Commissioner for Foods and Veterinary Medicine. As the question was being asked, I looked over at Mike and thought to myself, “he simply does not get paid enough to take this.” But, then again I thought, “heck he is a public servant. I suppose it simply comes with the territory.” But, I admit that I was surprised when he responded – politely – and with some details that I do not think he had ever talked about publicly. Mike explained that his career included time as a staff lawyer at the FDA in the mid 1970s and then practicing law during the 1980s at a law firm that represented Monsanto. He then returned to FDA in 1991 as Deputy Commissioner for Policy under Commissioner David Kessler. He then led FSIS from 1994 – 1996, where I first heard of him. In the late 1990s he was employed at Monsanto itself for 16 months, and beginning in 2000 he spent almost a decade in academia doing policy research related to food safety and African agricultural development. In 2009 he returned to lead the food side of FDA. Mike was candid with the fact that a history of moving in and out of government through the “revolving door” concerns people and can raise the question of whether his current role at FDA is conflicted by previous private sector roles. He explained to the questioner, that to guard against such conflicts, the government has clear rules about what a person can and cannot work on under those circumstances, and he follows those rules very carefully. For example, as Deputy Commissioner for Policy in the mid-’90s, Ethics Counsel said that he could work on general policy matters, such as policies for food labeling, but he was precluded from any involvement in specific product approvals of interest to Monsanto. So, he explained, among the mythologies surrounding his career was that he was involved in FDA’s decision to approve rBGH, the growth hormone used in dairy cows – he was not. Surprisingly, Mike was not done setting the record straight. I say surprisingly, because in all the years I have known him, I had never heard him speak to the issue. He went directly to concerns about his time at Monsanto, and the suggestion one can find readily on the Internet that he is now and always is “Monsanto’s man.” The questioner was by now a bit out of sorts when Mike said, “nothing is further from the truth.” Mike explained that while at Monsanto, he worked not as a “lobbyist,” but as the head of an internal think tank and as a policy advisor to senior management. In this role, he strongly advised Monsanto to drop its opposition to the labeling of biotech foods and to engage its external stakeholders in a more respectful and transparent way. Monsanto did not take his advice. He explained that he left Monsanto when it became clear that he would be unable to have any real impact. He realized that perhaps he was better suited to addressing issues that interested and concerned him from a more “objective platform,” which is why he spent the next decade in universities working primarily on policies affecting agriculture in Africa and food safety as a global public health and food system issue. Mike explained that he did not feel conflicted by his past experience with biotechnology policy, but he understood concerns about it and thus that the “baggage” he carries is real to some. That is why he has removed himself from participation in deliberations and decision making on all biotech-related issues that arise in the foods and veterinary medicine programs at FDA even though he has thoughts on it. Mike began to finish his answer with a bit of introspection – with the tone of someone at both the height of a career and also looking back. He said that he did his work at FDA every day with only one interest in mind, which is doing everything he can to fulfill the mission given by Congress to protect consumers and public health. He does this by working as closely as he can with stakeholders and partners, recognizing the need to find practical solutions that consider the wide range of perspectives on FDA issues held by the many people who care deeply about what FDA does. He said his only goal is to fully implement FSMA and address the range of other food safety, nutrition, and animal health issues central to the mission at FDA. This week, I had time to do just a little research. Frankly, it does not take long to find where Mike addressed biotech issues in writing on several occasions. This included a 2003 commentary in the Journal Nature Biotechnology (Vol. 21, No. 8, Aug. 2003) in which he criticized the aggressive approach the U.S. government and biotechnology industry were taking to promote biotech crops overseas, including in Africa, and argued that “the United States should be on the side of empowering choice” in the adoption of biotechnology, “in whatever way works in any given country,” including through labeling. He also called in that commentary for policy change aimed at strengthening pre-market oversight of biotech foods. In another article (Taylor and Cayford, American Patent Policy, Biotechnology, and African Agriculture: The Case for Policy Change, Harvard Journal of Law & Technology (Vol. 17, No. 2, Spring 2004), he argued, in the interest of African food security, for changes in U.S. patent policy and international patent agreements that would reduce the control Monsanto and other biotech companies could exercise over biotech crop improvements that could genuinely benefit food security. To me these are not exactly the perspectives of someone looking out for Monsanto’s interests. As the questions and answers wound down last week, I leaned over and asked Mike if he was up for a cup of coffee. Over a bad cup, I asked him why after all the years of being called “Monsanto’s Man” did he feel the need to say anything? He looked a bit perplexed at my question and said:

We’d all like to be judged for what we actually do rather than half-truths and myths on the Internet. I know I won’t satisfy those who object in principle to people working on FDA-related matters in both the public and private sector, or who think the rules governing these situations are not adequate, or who don’t like the policies FDA has made whether I worked on them or not. I fully understand and respect that point of view. About all I can say is that people in positions like mine work in the open, under the guidance and scrutiny of their bosses and many others, and I have always done my best to fulfill my responsibilities to FDA and its public health mission.

I am not sure we can ask more of Mike or anyone in government.

  • Great article, and long overdue. No one ever seems to get these points across, and people continue to spread the idea that Mr. Taylor is some kind of Monsanto lackey. It’s nice to see a summarization of the facts that demonstrate he has been critical of the biotech industry and careful about what he works on at FDA.

  • I can only hope this shows up in the 1st page of Google search results.

  • Nick Meyer

    Hmm. Since all these people with former Monsanto ties like he and Clarence Thomas and Tom Vilsack got into their current positions, GMOs have gotten a free pass and the voice of the people in opposition (90 percent want labeling at the very least) has been silenced. Must be a coincidence then because of a few short sentences spoken by the guy. Kind of like how Obama pledged to label GMOs, pledged to veto the NDAA, and did neither. We go by actions not what someone says in a random interview. Do the right thing or you will be justifiably labeled a GMO loving Monsanto lackey who is corrupting the very nature of nature and quite possibly our health.

    • Right. Everyone who doesn’t agree with you on GMOs is a corporate lackey. If you don’t agree with us, you are a lackey and a “traitor,” right? You are fighting a righteous cause. That is the biggest meme of the anti-GMO crowd. It’s not possible you might be mistaken or heaven forbid, wrong about the GMO issue. Such is the mind of the true believer.

      Reagan once said, “Facts are stupid things” and it seems the anti-GMO movement has adopted that belief. Your reaction to Taylor’s answers just goes to show that you’re not interested in the facts but maintaining your worldview. You have reduced a man’s entire career based on one company he worked for. So, now everything he has ever done or will ever do is tarred with that accusation.

      You trot out the 90% figure. So, I guess because the majority wants something it should be a law? The majority of Californians voted down gay marriage. Should we have listened to that majority? What are they doing going to court over the vote? The people have spoken, right?

  • Susan Rudnicki

    Mr Marler—I am glad you have written this clarifying article regarding Mr Taylor. But please spare us all the tone of injured fealty when you describe the journalist digging into the “myths” of Taylor’s employment. All too often, that suspiciousness we have in the public realm is completely justified, but the media typically mouths whatever slant the government agencies put out there as “the facts”, in effect doing nothing to ellucidate the facts. I invite you to refer to the work of the scrappy little NGO, Project on Government Oversight—or POGO, as a introduction into the vicious PR spin hype and abuse of government/private industry whistleblowers that much more commonly reigns as “policy” in our country. These exposes’ detail with great rigor the burying of criminal evidence of misconduct, the flagrant misuse of taxpayer dollars, and the hounding and prosecution of honest government employees when they dare to come forward with their misgivings in all areas of government involvement.

    Mr Taylor may have argued “in the interest of African food security, for changes in U.S. patent
    policy and international patent agreements that would reduce the control
    Monsanto and other biotech companies could exercise over biotech crop
    improvements that could genuinely benefit food security. To me these are
    not exactly the perspectives of someone looking out for Monsanto’s

    as you report. However, knowing the policies and heavy handed industry driven actions carried out at the USDA over the last 30 years, I say the process is a lot more corrupt at a deeper level than “changes in patent policy” My brother worked at the Foreign Markets development division at USDA for 30 years and I saw first hand through him, the push to get the rest of the world adopting our filthy, unhealthy, unsustainable models of producing meat, grain, and sugars. The push to open markets in countries failing “to eat like us” yet, is relentless and driven largely by the profit motive to gain US producers a bigger share for export.

    Further, the “revolving door” (the issue is taken up by POGO directly in this month’s communications, should you be interested) is a blatant and furiously debated injury to the public trust, ongoing and expanding. Private corporate concerns insert themselves into every area of supposedly “conflict of interest free” public policy and investigation. I am sure you are not unaware of this issue, but from my point of view, it is a worsening trend as the world becomes ever more “globalized in the supply chains” and more profit is to be gained by ever larger consolidations of capital.

    For example, regarding the importance of honeybees in American agriculture, there exists a perfect example of the corruption of the public’s interest in the “investigation of the causes” of CCD, (colony collapse disorder) afflicting important pollinators. The EPA has granted the exclusive research investigative program to Bayer Crop Science, the manufacturer of the most implicated class of chemicals (neonicotinoids) in killing honeybees worldwide. This government policy decision and obviously blatant collusion infuriates honeybee keepers, like myself, and leads to ever declining regard for the government’s interest in being a protector of the public.

    So, I agree with Mr Taylor in his observation that ” those who object in principle to people working on FDA-related matters
    in both the public and private sector, or who think the rules governing
    these situations are not adequate, or who don’t like the policies FDA
    has made whether I worked on them or not. I fully understand and respect
    that point of view” He at least recognizes we citizens right to protest the policy decisions and his obligation to honestly address the questioning. But as I detail above, the base decision making models and entanglements of money and profit, are rotten at the core. THAT is what I will work on as a private taxpaying citizen.

  • Oginikwe

    Maybe, Mr. Marler, your judgement is clouded by your friendship.

    Mr. Taylor, more often than not, has acted in the best interests of the corporations. rBGH which is banned in 27 countries. The EU’s report on this says it all. So, exactly why should we trust this gentleman and what he says rather than what he has done?

    EU’s “Report on Public Health Aspects of the Use
    of Bovine Somatotrophin” (3/16/1999) : http://ec.europa.eu/food/fs/sc/scv/out19_en.html

  • Sharon

    You are likely paid by the big agriculture industry to write this. This is definitely not unbiased reporting, if you can even call it reporting. It’s almost silly. How does Michael Taylor get an agency in government made up just for him? after his stint at the FDA. Why do they always make policy in favor of Monsanto, creator of Agent Orange, PCBs, Dioxin, etc.

  • doc_raymond

    Excellent post. Taylor has always been a hero of mine. Thanks for trying to set the record straight

  • You’re a regular commenter here, so I’ll respond. Do you ascribe rBGH’s approval to Taylor despite the fact that he purposefully did not get involved in FDA’s work on rBGH (specifically because he had worked for Monsanto)?

    As part of unrelated research, I was just reading an article on food safety regulation of which Taylor was a co-author. It singled out GMOs as having the potential to present new food safety risks, thus suggesting the need for ongoing scrutiny. This is hardly complicit with biotech supporters’ claims that GMOs are proven safe and burdened by overregulation.

  • your run on WAY too long bro………..

  • We can ask them to observe simple business ethics and avoid any appearance of conflict of interest. Do you think he is the only individual qualified to perform his job at the FDA? One that was created only recently by President Obama. Quite simply, he just shouldn’t be there, it looks shady.

  • TheTruth

    B.S.! Why isn’t he doing his job and looking out for the health of the general public, then?? He should be standing in the way of GMO Salmon. Why did he do to stop the unconstitutional, illegal Monsanto Protection Act from being passed? What did he do to support GMO labeling?

    • Dennis Boylon

      He did nothing to support labeling. Even though in this article he claims he lobbied Monsanto senior leadership to do it. I cry BS

  • Cyn Doyle

    I’m sorry, but your PR for Michael Taylor didn’t sway me one iota.

    Mr. Marler, please pass this message on to your friend and all of his friends:

    Michael Taylor- You and all of Monsanto’s other government “infiltraitors” (spelled like that purposefully) should NOT be working at OUR FDA. We need people in our government who will REALLY protect us by putting our interests BEFORE corporations.

    Give us Independent testing (lab chosen by Jill Stein of the Green Party as she has zero dealings with Monsanto) of ALL GMO products. Results MUST be publicized on video along with the full study as it actually happens.

    If you want public trust, earn it or are you just so bought and sold that you just don’t care at all what we, the people, want?
    Is the crinkling sound of the corporate cash drowning out the people’s voices?

    Help us help you, that is if you want to keep your jobs. Those of you with any prior connections whatsoever with Monsanto or any other GMO company will be forced out of our government, in any case. It’s a SEVERE conflict of interest.

  • Dennis Boylon

    I think this article is more damning of him myself. He admits he has some concerns over Monsanto practices and labeling. What has he ever done to confront Monsanto about this? Run away and work a cushy government job? When has Michael Taylor ever stepped up to a powerful corporation like Monsanto? He doesn’t. He even admits he doesn’t. He brags he left because he couldn’t change anything but that his heart was in the right place. He will persecute Amish farmers for selling raw milk though. Of course they don’t have a powerful lobby in DC so it is safe for him to send armed men to face down the Amish. He is also trying to enact this farm to table tracking system that will mean more small farmers going out of business. These laws are passed to supposed objection by big agribusiness but it is a farce. They want the new regulations because it drives out the small farmer and gives them the whole market. They will be able to set prices after the small farmer is driven out.



  • Goes Hotbed

    The Hidden agenda about Monsanto. Take A long look is all the funds reported,and who.


  • Michael Taylor

    Judge him on what he does rBGH = obesity epidemic

    • Sterling Ericsson

      Your comment shows you didn’t even read the article.

      “So, he explained, among the mythologies surrounding his career was that he was involved in FDA’s decision to approve rBGH, the growth hormone used in dairy cows – he was not.”

      Shame on you.

  • Archibald_Bomwitz

    Saying one thing publicly and working behind the scenes for the direct opposite are not unheard of practices!

  • Clayton Barlow

    Crap piece. Do your homework and next time you “bump” into Taylor ask him about how he manipulated the system to get rBGH passed. Ask him about the fact he knows that e-coli is exacerbated by feeding corn to cattle and grass fed beef don’t have the same issues. Or maybe just ask him if his family avoids GMO’s (which he has been caught saying)

  • grn1

    Marler has also made $$$$$$$$$$$$$$$$$$ on e.coli death and infection. Why shouldn’t a representative of this government have to answer questions regarding food safety. Only marler would question and then represent himself as go to guy on food safety. Yes Bill we can ask more and expect it. We the citizens pay for it dearly. You kept me on the phone waiting 20 years ago but refused to know the truth yourself. Such greed masked in concern.

  • gomurr

    Do you really understand what GMOs are and how they’re created? You do realize it’s not like simply breeding a better tomato.

    I say this with all due respect, as it’s been my experience most people tend to equate GMOs in their mind, with hybrids. They know nothing of the genetic manipulation, how it’s facilitated, nor are they aware of it’s unknown potential to mutate with undesirable results while hanging out in your intestines.

    While there are others, Monsanto is the worlds largest supplier of GM seeds. They sold these seeds to the farmers by convincing them, not only of far greater yields, but because they would require far less herbicides. These were known as Roundup Ready crops.

    The first question you must ask yourself, is why would a chemical company such as Monsanto deliberately cut a huge % of their Roundup profits by giving farmers something that required less of it? They wouldn’t, of course. In fact, what has happened is we now have a new mutant strain of “super weeds” who have become immune to Roundup. As a result, crops are now being sprayed with heavier and heavier doses of Roundup, often to the point of saturation. To add insult to injury, not only do GMO crops fail to live up to their promises of high yields of nutritious food to feed the planet, farmers may not save seeds as was traditionally done, but must purchase them from Monsanto yearly.

    Without going much further, half of Roundup is glyphosate. Glyphosate was once part of another “safe product” known as Agent Orange. Turns out it wasn’t very safe. It didn’t stop them from denying it year after year while large numbers of Vietnam vets suffered the ill effects of exposure to AO. A week, or so ago, the “cancer” branch of WHO, known as the International Agency for Research on Cancer (IARC), admitted that it’s “most likely” glyphosate is a carcinogen.

    If you find it necessary to spray your garden, or purchase food sprayed with a herbicide, a thorough cleansing will remove the residue. When you eat something that’s Roundup Ready, there’s no way to do this. The herbicide has been genetically inserted in your potato. It is IN your potato, not ON it.

    While it’s very possible Michael Taylor has made every effort to remain above board in his position at the FDA, his work for African food security was funded by the Rockefeller foundation and also involves Monsanto and the Gates Foundation. His dealings with Monsanto, the USDA, and FDA given the impression of cronyism and provide a basis for conflict of interest. At any rate, as Deputy Commissioner of Policy at the FDA, he would have been aware that when it came to Monsanto, there was no policy. They were given free reign to police themselves for years by the FDA, with the FDA only requiring that Monsanto “inform’ them as to the safety of GMOs.

    Most of our government agencies have become revolving doors for the chemical and the pharmaceutical companies. Anyone who believes there is nothing wrong with this and there is no serving of special interests here, needs to face facts. Neither the USDA, the FDA, Monsanto, or anyone else, cares if our food is “safe”. If they did additives such as MSG, formaldehyde, high fructose corn syrup, and aspartame, among others, would be banned. There would be no fluoride in our water, no rbGH in our milk, no antibiotics or hormones in our meat. Drugs with known, but downplayed, lethal side effects, would not be approved until such a time the anticipated “collateral damage” would be too much to ignore, at which point it would be taken off market.

    If you still this there’s no collusion here, ask yourself why OUR elected Congress passed something as diabolical as the Monsanto Protection Act, disallowing farmers whose soil/crops had been contaminated by Monsanto’s GMO seeds, to seek compensation, but ALLOWING Monsanto to sue the farmer for illegally possessing/using their copy righted seed without permission or compensation. Rather than protect the citizens, they choose to protect the poisoner of the planet.