Consumer Reports | Food Safety News https://www.foodsafetynews.com/author/consumerreports/ Breaking news for everyone's consumption Wed, 26 Apr 2023 21:50:01 +0000 en-US hourly 1 https://wordpress.org/?v=6.3.1&lxb_maple_bar_source=lxb_maple_bar_source https://www.foodsafetynews.com/files/2018/05/cropped-siteicon-32x32.png Consumer Reports | Food Safety News https://www.foodsafetynews.com/author/consumerreports/ 32 32 Letter to the Editor: CR supports USDA work to make chicken safer https://www.foodsafetynews.com/2023/04/letter-to-the-editor-cr-supports-usda-work-to-make-chicken-safer/ https://www.foodsafetynews.com/2023/04/letter-to-the-editor-cr-supports-usda-work-to-make-chicken-safer/#respond Thu, 27 Apr 2023 04:04:00 +0000 https://www.foodsafetynews.com/?p=226984 — OPINION — Consumer Reports is supporting a proposal announced April 25 by the USDA to declare salmonella an adulterant in breaded stuffed raw chicken products at low levels so that the agency can more effectively respond to foodborne illness outbreaks. CR praised the proposed rule as an important first step to address widespread salmonella contamination and... Continue Reading

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— OPINION —

Consumer Reports is supporting a proposal announced April 25 by the USDA to declare salmonella an adulterant in breaded stuffed raw chicken products at low levels so that the agency can more effectively respond to foodborne illness outbreaks. CR praised the proposed rule as an important first step to address widespread salmonella contamination and is encouraging the agency to adopt additional measures to protect the public from the dangerous bacteria in other chicken products. 

“Far too many people get sick every year from poultry contaminated with salmonella bacteria that could be avoided with stricter industry prevention practices,” said Brian Ronholm, director of food policy for Consumer Reports.  “The USDA’s proposal on salmonella in breaded and raw chicken products is a very encouraging formal step in the process, and it demonstrates they are serious about pursuing measures aimed at reducing Salmonella illness rates. We look forward to working with USDA to quickly move this forward.” 

Breaded raw stuffed chicken products include some chicken cordon bleu and chicken Kiev products found in the freezer section of the grocery store.  These products may appear cooked to consumers but they contain raw chicken and are only heat-treated by manufacturers to set the batter or breading.

Under the proposal announced today, breaded and stuffed raw chicken products would be considered adulterated if they tested positive for Salmonella at 1 colony forming unit (CFU) per gram prior to stuffing and breading.  The adulterated designation would require companies to recall any product that tests positive above this low level of contamination, instead of waiting for outbreaks when people get sick.  

Salmonella is widespread in chicken in part because of the often crowded and filthy conditions in which they are raised. A recent CR investigation, for example, found almost one-third of ground chicken samples tested contained salmonella.  Nearly 1.35 million Americans get sick from salmonella every year, about one-fifth of those cases come from chicken or turkey.

While the USDA requires producers to test poultry for salmonella, a processing facility is allowed to have the bacteria in up to 9.8 percent of all whole birds it tests, 15.4 percent of all parts, and 25 percent of ground chicken. Producers that exceed these amounts are given what amounts to a warning, but not prevented from selling the meat.

Consumer Reports has called on the USDA to set more aggressive goals to sharply reduce the percentage of chicken samples allowed to test positive for salmonella and to focus on reducing the salmonella strains that pose the biggest threat to human health. CR also believes the USDA needs more authority to inspect poultry plants and should close facilities immediately when high salmonella rates are found.

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House report on baby food shows FDA, companies must take action now https://www.foodsafetynews.com/2021/09/house-report-on-baby-food-shows-fda-companies-must-take-action-now/ https://www.foodsafetynews.com/2021/09/house-report-on-baby-food-shows-fda-companies-must-take-action-now/#respond Thu, 30 Sep 2021 04:07:01 +0000 https://www.foodsafetynews.com/?p=207820 Opinion Consumer Reports today (Sept. 29) urged baby food manufacturers and the Food and Drug Administration to take quick and decisive action to address the “disturbing” findings in a new report issued by the U.S. House Oversight Committee. Oversight’s Subcommittee on Economic and Consumer Policy released a new staff report that shows “high levels of toxic heavy... Continue Reading

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Opinion

Consumer Reports today (Sept. 29) urged baby food manufacturers and the Food and Drug Administration to take quick and decisive action to address the “disturbing” findings in a new report issued by the U.S. House Oversight Committee.

Oversight’s Subcommittee on Economic and Consumer Policy released a new staff report that shows “high levels of toxic heavy metals in baby food and the industry’s failure to end harmful practices that pose serious health risks to babies and toddlers.” The report also has recommendations for FDA and industry to eliminate toxic content in baby foods. The subcommittee issued an initial report in February 2021.

Brian Ronholm, Director of Food Policy for Consumer Reports, said, “What’s especially disturbing about the report’s findings is the industry’s dismissive approach toward ensuring the safety of baby food.

“Between incomplete recalls, weakening their own standards, and the refusal to test finished products, these baby food manufacturers do not appear to be putting safety first. This report clearly demonstrates the need for the FDA to act quickly in publishing maximum limits for toxic heavy metals in baby food and requiring the industry to perform finished-product testing. The findings demonstrate that today’s rules and industry promises are woefully inadequate when it comes to safety.”

In 2018, Consumer Reports’ food safety team analyzed 50 nationally distributed packaged foods made for babies and toddlers, checking for cadmium, lead, mercury, and inorganic arsenic, the type most harmful to health.  CR’s tests found that about two-thirds (68 percent) had worrisome levels of at least one heavy metal.

Fifteen of the foods would pose potential health risks to a child regularly eating just one serving or less per day. Snacks and products containing rice and/or sweet potatoes were particularly likely to have high levels of heavy metals.

For years, CR has advocated for regulations, legislation, and industry reforms to reduce toxins in baby food. CR has endorsed the Baby Food Safety Act introduced in Congress, which would set strict limits on heavy metals in baby foods.

(To sign up for a free subscription to Food Safety News, click here.)

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Consumer Reports maintains stand on possible dangers of meat, poultry https://www.foodsafetynews.com/2018/09/consumer-reports-maintains-stand-on-possible-dangers-of-meat-poultry/ https://www.foodsafetynews.com/2018/09/consumer-reports-maintains-stand-on-possible-dangers-of-meat-poultry/#respond Sun, 02 Sep 2018 04:03:01 +0000 https://www.foodsafetynews.com/?p=176140 Opinion Note on the author: James Rogers, Ph.D., is director of food safety testing and research at Consumer Reports. He submitted this opinion piece, originally titled “Let’s Keep It Honest: The Full Story on Drug Residue in Meat & Poultry Testing,” in response to FSIS Administrator Carmen Rottenberg’s Aug. 29 alert on this topic. In recent... Continue Reading

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Opinion

Note on the author: James Rogers, Ph.D., is director of food safety testing and research at Consumer Reports. He submitted this opinion piece, originally titled “Let’s Keep It Honest: The Full Story on Drug Residue in Meat & Poultry Testing,” in response to FSIS Administrator Carmen Rottenberg’s Aug. 29 alert on this topic.


In recent days, a Consumer Reports investigation indicating that potentially dangerous and banned substances have made their way into our meat supply has been called into question by industry organizations and the USDA’s Food Safety Inspection Service (FSIS). We took a hard look into the presence of drugs, including chloramphenicol, an antibiotic linked to potentially deadly anemia; phenylbutazone, an anti-inflammatory deemed too risky for human use; and ketamine, a hallucinogenic party drug and experimental antidepressant. 

What we found is deeply worrisome and is why CR believes greater consideration is warranted on behalf of all consumers.

As a scientist and former FSIS official, I intimately understand how the agency collects, tests, and measures contaminants in food. When we looked at testing data from the FSIS, both an initial and then revised set, serious concerns came to light about the process, the standards applied, and the findings themselves.

At the heart of the matter is that there should never be any of these banned substances in the food supply. In the case of this testing, the FSIS created what can only be called an arbitrary and self-determined threshold, far above the legal threshold for the drugs chloramphenicol, ketamine, nitroimidazoles, and phenylbutazone, which is zero and what the Food, Drug, and Cosmetic Act mandates.

The FSIS has attempted to redirect the conversation about CR’s investigation to make it about the completeness of the data, offering up the explanation that the initial data was preliminary and released in error, and should be dismissed. The meat industry has, not surprisingly, supported that position.

Here’s the truth: the initial data set recorded thousands of data points showing detectable amounts of drugs in meat samples. The revised set issued by FSIS, using their arbitrary threshold, showed many of the results changed to “Residue Not Detected.” However, when the results that did remain were compared to the initial set, near-identical results appeared, including down to the final decimal place. The only scientific conclusion we can draw is that the entire initial data set is both real and meaningful; in many cases, trace amounts were no longer included simply because they did not meet the FSIS’s arbitrary threshold.

Upon consideration by CR scientists, and after several exchanges we had with the FSIS regarding the methods used to create both data sets, the FSIS was unable to provide a scientifically convincing rationale for why the data should be dismissed. In fact, the process used by the FSIS to set their threshold has been cloaked in secrecy, neither shared publicly, nor peer reviewed.

The criteria applied by the FSIS to the results in question do not meet established scientific methods, including peer review. They are also less rigorous than the criteria used by other government agencies, including the FDA and the EPA. 

That’s why CR’s only mission is to work with and for the consumer, to keep us all safe and healthy. We are calling for more discussion within the regulatory and scientific community on how to better our food system and stand by the principle of zero tolerance for potential consumer harm from banned drugs in meat. The FSIS and the entire food industry should operate by that principle, too.

Because no consumer has a way to determine what’s inside the meals we eat — the ability to analyze food on our own — we all must be able to rely on the promises of producers, the safeguards of government standards, and the scientific tests of independent experts to ensure our safety. 

(To sign up for a free subscription to Food Safety News, click here.)

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Antibiotic Resistance: Very Critical to Your and My Health https://www.foodsafetynews.com/2013/01/antibiotic-resistance-very-critical-to-your-and-my-health/ https://www.foodsafetynews.com/2013/01/antibiotic-resistance-very-critical-to-your-and-my-health/#comments Tue, 22 Jan 2013 06:03:17 +0000 https://www.foodsafetynews.com/?p=63648 The scientists here at Consumer Reports read Dr. Richard Raymond’s op-ed “Antibiotics and Animals Raised for Food: Lies, Damn Lies and Statistics” with great interest. We were particularly struck by his assertion that most antibiotics used in animal production are not used to treat humans and are therefore “not critical to your or my health.”... Continue Reading

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The scientists here at Consumer Reports read Dr. Richard Raymond’s op-ed “Antibiotics and Animals Raised for Food: Lies, Damn Lies and Statistics” with great interest. We were particularly struck by his assertion that most antibiotics used in animal production are not used to treat humans and are therefore “not critical to your or my health.” This claim is not scientifically justifiable. While it is true that not all of the antibiotics used in food animal production are used in human medicine, a majority of them belong to the same drug “classes”. Antibiotics in the same class often work to stop the growth of bacteria by using a similar mechanism of action. This becomes important when you consider the scientific principles of cross-selection and co-selection. Cross-selection means that the gene for resistance to one antibiotic will often also confer resistance to other antibiotics in the same class that work by the same mechanism of action. So giving one antibiotic to an animal that may not be used in human medicine may lead to the development of a bacteria resistant to an antibiotic in the same class that is used in human medicine. For example, cepharin (first generation cephalosporin) is used to treat mastitis in cattle but not used in human medicine, while cephalexin (first generation cephalosporin) is used in human medicine to treat Staphylococcus aureus. Bacteria that become resistant to cepharin, due to overuse in cattle, will also be resistant to cephalexin. Interestingly, Dr. Raymond cites cephalosporin as an antibiotic critical to human health. Another important principle is co-selection, where multiple resistant genes can be transferred together, because they are physically located next to each other in the bacteria’s genetic material, either the main chromosome or extra-chromosomal DNA. This means that feeding a specific antibiotic to food animals that is not used in human medicine could actually lead to the development of bacteria that are resistant to other antibiotics in different classes that are important in human medicine. Yet despite these scientific principles, Dr. Raymond believes “that the majority of antibiotics used in animals are of little or no importance to me as a physician or a grandparent.” However, the basic point he misses is that bacterial species can readily swap resistance genes with each other and bacteria in other species, genera and even other families–hardly of “little or no importance.” That resistance is accelerated and amplified by feeding healthy animals low doses of antibiotics everyday. When it comes to antibiotics like tetracyclines, unlike Dr. Raymond, we agree with the World Health Organization that there is a benefit to guarding their effectiveness. Tetracyclines are used against infectious diseases, including chlamydia, typhus, syphilis, Lyme disease, Legionnaire’s disease, malaria, Rocky Mountain Spotted Fever, cholera and the bubonic plague. Bacterial resistance to tetracycline was identified as early as the 1950s, the FDA tried to ban the use of tetracycline for growth promotion purposes in animal production as far back as 1977, and in 1986, Sweden prohibited the use of antibiotics including tetracycline for growth-promotion purposes. All of Europe followed in 2006. In this country, however, we have continued to allow tetracycline and other antibiotics to be fed indiscriminately for growth promotion purposes to healthy animals everyday. It remains to be seen if FDA’s 2012 request to drug producers and the livestock industry to voluntarily phase out this use by 2015 will produce any real reduction in antibiotic use in food animals. Dr. Raymond spends a lot of time focusing on the amounts of antibiotics used in humans versus animals. The fact that the inappropriate use of antibiotics–regardless of whether or not they are used in humans or animals–leads to an acceleration of the development of antibiotic resistance is a scientific fact. We agree with Dr. Raymond that the overuse of antibiotics in human medicine is an important issue. But since the same science that applies to the overuse in humans also applies to animals, we can not understand why he does not see overuse of these important drugs in animals as a problem. As for the exact numbers of how many antibiotics are used in food animal production—that data isn’t well disclosed to the public and is the subject of much debate. Dr Raymond uses his own numbers of unknown (or not easily obtainable) origin, which introduces a lack of transparency in his analysis. This is why groups like Consumers Union, the policy and advocacy arm of Consumer Reports, are supporting legislation to make this information readily available to everyone. Finally to answer Dr. Raymond’s question: “So when you read a report funded by Consumers Union, stating that they found Salmonella sp. bacteria resistant to Cipro (a fluoroquinolone), where do you think that resistance came from?” The answer is not–as Dr Raymond implies– from the human use of Cipro. Salmonella is a bacteria found on chicken or pork and not normally on humans. Salmonella therefore will have only been marginally exposed to all those flouroquinolones used in humans, compared to the flouroquinolone use in animals. So, resistance to cipro found in Salmonella from pigs or chickens, is likely due to use of flouroquinolones in animal agriculture not human medicine. Flouroquinolones were approved for all uses in poultry production in 1996 but were banned in 2005 because resistance rates went up after use. As one of the few independent consumer organizations that has been regularly testing meat and poultry for pathogens and antibiotic resistance for fifteen years, we believe that the the routine daily administration of antibiotics to animals is dangerous for public health. The problems and consequences of amplifying antibiotic resistance from feeding healthy animals antibiotics everyday is hardly a “Lie” or a “Damn lie”—it is a serious problem—a problem that was not invented by consumer organizations. In fact, groups like WHO, FDA, CDC, the EU, and medical and public health communities have all acknowledged the importance of addressing this issue. Healthy people don’t eat antibiotics everyday and neither should animals. It’s time for the industry to stop making excuses and stop inappropriately using these medically important drugs. Truth and Transparency: Unlike Dr. Raymond, Consumer Reports accepts no money from the antibiotic industry or any industry for that matter. Since 1936, Consumer Reports has been singularly focused on the consumer interest and refuses advertising, free samples, and corporate contributions. It is supported by the sale of its products and services and donations from consumers and foundations.Urvashi Rangan, PhD is an environmental health scientist and toxicologist. She leads Consumer Reports’ Consumer Safety and Sustainability Group and serves as the Executive Director of its Food Safety and Sustainability Center. Dr. Rangan directs all of the organization’s scientific risk assessments related to food and product safety, which she translates into actionable recommendations for both lawmakers and consumers. Most recently, she was the architect of the organization’s studies of arsenic in apple juice and rice and is a national expert on labels. Michael K. Hansen, PhD is a Senior Scientist with Consumers Union, the policy and advocacy arm of Consumer Reports. He works primarily on food safety issues and has been largely responsible for developing the organization’s positions on the safety, testing and labeling of genetically engineered food and “mad cow” disease. Dr. Hansen served on the USDA Advisory Committee on Agricultural Biotechnology from 1998-2002, and on the California Department of Food and Agriculture Food Biotechnology Advisory Committee, from 2001-2002. Michael Crupain, MD, MPH is the Director of Consumer Reports’ Food Safety and Sustainability Center where he directs the day-to-day operations of the organization’s food-safety testing. He joined Consumer Reports in 2012 and is a trained physician in Preventive Medicine with expertise in public health-based risk assessment. Dr. Crupain received his Masters in Public Health from the Johns Hopkins School of Public Health, where he is also an adjunct professor.

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