Health
Food Safety Jeopardized by Onslaught of Funding and Staff Cuts

In the last few years, foodborne pathogens have had devastating consequences that alarmed the public. Bacteria in infant formula sickened babies. Deli meat ridden with listeria killed 10 people and led to 60 hospitalizations in 19 states. Lead-laden applesauce pouches poisoned young children.
In each outbreak, state and federal officials connected the dots from each sick person to a tainted product and ensured the recalled food was pulled off the shelves.
Some of those employees and their specific roles in ending outbreaks are now threatened by Trump administration measures to increase government efficiency, which come on top of cuts already being made by the Food and Drug Administration’s chronically underfunded food division.
Like the food safety system itself, the cutbacks and new administrative hurdles are spread across an array of federal and state agencies.
At the Food and Drug Administration, freezes on government credit card spending ordered by the Trump administration have impeded staff members from buying food to perform routine tests for deadly bacteria. In states, a $34 million cut by the F.D.A. could reduce the number of employees who ensure that tainted products — like tin pouches of lead-laden applesauce sold in 2023 — are tested in labs and taken off store shelves. F.D.A. staff members are also bracing for further Trump administration personnel reductions.
And at the Agriculture Department, a committee studying deadly bacteria was recently disbanded, even as it was developing advice on how to better target pathogens that can shut down the kidneys. Committee members were also devising an education plan for new parents on bacteria that can live in powdered infant formula. “Further work on your report and recommendations will be prohibited,” read a Trump administration email to the committee members.
Taken together, there is concern in the food safety field that the number of outbreaks could grow or evade detection. By limiting resources, the cutbacks pare back work meant to prevent problems and to focus efforts on cases in which someone was already hurt or killed, Darin Detwiler, a food safety consultant and associate professor at Northeastern University, said. His toddler son died in an E. coli outbreak in 1993.
“It’s as if someone, without enough information, has said, What’s a good way to save money on our automobiles?” he asked. “Let’s just take out the seatbelts and airbags, because do we really need them?”
Robert F. Kennedy Jr., the nation’s health secretary, has a keen interest in food. He has already pledged to get color additives out of food and started an effort called “Operation Stork Speed” to examine the nutritional content and potential toxins in infant formula. Yet some of the most dangerous food problems in recent years have been from pathogens.
Last year, nearly 500 people were hospitalized and 19 died from foodborne illnesses with a known cause, double or more than in the year before, according to the U.S. P.I.R.G. Education Fund, an advocacy group. (Most food poisoning is never reported or traced back to a particular food.)
Government cutbacks affect a number of areas that officials were shoring up to prevent repeats of recent outbreaks. Here are the details of some of the changes:
Key committees shut down
Often in response to a deadly outbreak, a joint F.D.A. and Agriculture Department committee dived into the details to seek ways to improve detection and to limit illness and death. The committee has also examined how to deploy rapidly changing technology — including artificial intelligence and genome sequencing — to protect public health.
The Trump administration abruptly shut down the committee earlier this month, citing the executive order on reducing government bureaucracy. It demanded that work stop for the panel called the National Advisory Committee on Microbiological Criteria for Foods and also for the National Advisory Committee on Meat and Poultry Inspection.
The microbial committee was studying how to more accurately identify infants who would be most at risk from cronobacter sakazakii, the deadly bacteria that contributed to the decision to temporarily shut down an Abbott Nutrition infant formula plant in Michigan in 2022. The committee planned to then provide advice to caregivers who should use sterile liquid formula instead of powdered formula, which is not sterile.
Abby Snyder, a Cornell University food scientist and co-chair of a subcommittee on infant formula, said she was disappointed by the decision to discontinue the committee’s work. “Safety of powdered formula for infants is of critical importance and I think important to most people,” Dr. Snyder said.
The F.D.A. did not respond to a question about whether Kyle Diamantas, its food division chief, was involved in the decision to axe the committee. A former corporate lawyer, Mr. Diamantas worked on cases defending Abbott over claims of harm related to infant formula.
Michael Hansen, a scientist and member of the committee from Consumer Reports, an advocacy group, said his team on the committee was trying to pinpoint certain types of E. coli that were most likely to cause bloody diarrhea and kidney failure, among other efforts.
He said the decision to end the committee was a shock and destroyed almost two years of work on harnessing genomic sequencing — technology that is now widely available and affordable — to limit outbreaks. The team leveraged hours of volunteer work from the top experts in the field, he said.
“It makes no sense that they were getting rid of this committee,” Dr. Hansen said, “because if you want to do a full cost-benefit analysis, all the work that we were doing was actually free of charge.”
Spending freezes
Scientists at the F.D.A.’s product and food testing labs said they were barred from some routine use of their government credit cards because of an executive order backing the efforts of Elon Musk’s so-called Department of Government Efficiency.
An exception has been made for “critical activities,” an F.D.A. spokeswoman said.
That has slowed or stopped some testing of grocery items for hazardous bacteria and monitoring of shellfish and food packaging for PFAS, chemicals linked to cancer and reproductive harm.
Credit cards can be used in an investigation of listeria in frozen supplemental shakes dispensed in elder care homes that have been linked to a dozen deaths. For other work, staff members have encountered red tape, agency scientists said.
“Even hours can matter in an outbreak,” said Susan Mayne, an adjunct professor at Yale School of Public Health and a former F.D.A. food official who had heard from current employees about the situation. “Any delay is unacceptable when you’re dealing with a product that can kill someone.”
Food safety inspections
In a recent letter to lawmakers, F.D.A. officials said that the agency employed about 443 food safety inspectors — far fewer than the agency needed to inspect every food processing facility at the pace Congress mandated. The agency estimated that it would need about 1,500 more workers to inspect 36,600 food facilities, foreign and domestic, once every five years or once every three years for high-risk producers.
At this time, those inspectors are largely exempted from losing their jobs.
However, one team of outbreak investigators is vulnerable, according to Jim Jones, the agency’s food division chief in the latter part of the Biden administration. This team, known as CORE, coordinates with the Centers for Disease Control and Prevention to link a cluster of sick people to a specific food plant or farmer’s field. The team tracks inspections and efforts to ensure that tainted food is removed from store shelves.
Mr. Jones said the team was recently built up as a fully remote operation that would most likely be affected when orders to return to work at federal offices were put in place this month. Workers who live more than 50 miles from an F.D.A. office have until late April to begin working at a federal site.
“So their choices will be you either move so that you can go to a federal facility, or you leave,” Mr. Jones said. “There’s nothing strategic about who gets caught in that pickle.”
Across the F.D.A., inspections plummeted during the pandemic and have not returned to the higher levels before 2020. At the same time, the amount of imported food has risen, including clams that have repeatedly found to be contaminated with PFAS.
Cutbacks to States
Once the F.D.A. identifies a factory that was the source of contamination, it often relies on state inspectors to investigate on site. In criticizing the reductions, Senator Richard Blumenthal, Democrat of Connecticut, pointed out that state inspectors performed about half of the inspections at food processing facilities, 90 percent of the produce safety inspections and all of the retail store visits.
The F.D.A. also turns to state and local public health officials to pluck potentially tainted foods from grocery store shelves and test them at a network of 55 public health labs throughout the United States. If a product is recalled, the state officials also audit grocery stores to be sure the food has been removed.
A move late in the Biden era sharply limited the funding that the F.D.A. sends to states and to the labs that do critical work. The latest $34 million funding reduction applies to states and to those public health labs. The agency said in a letter to Mr. Blumenthal that the cuts were being made because the food division had a flat budget and costs were increasing because of inflation.
Thom Petersen, commissioner of the Minnesota Department of Agriculture, said F.D.A. food safety funding had fallen steadily since 2019, with the latest cut striking deeper and possibly leading to layoffs. He said the funding loss could slow the important work of taking bad food out of stores.
That work proved particularly important after officials discovered extremely high levels of lead in cinnamon in applesauce pouch snacks for children. The F.D.A. ended up sending a warning letter to Dollar Tree over its failure to quickly pull the pouches.
“Timing is the important piece,” Mr. Petersen said. “We want to take care of those and work on that.“
The public health labs reported that the money amounted to about 30 percent of their funding, which helps them respond to outbreaks more quickly than the F.D.A.
In the Boar’s Head listeria outbreak, for instance, lab officials in Maryland and New York bought liverwurst at stores that tested positive for the same strain that sickened people. A trade group for the labs predicted that the budget cuts could delay responses — and lead to more people getting sick.

Health
Video: Trump Pushes Unproven Link Between Tylenol and Autism

new video loaded: Trump Pushes Unproven Link Between Tylenol and Autism
By Azeen Ghorayshi, Claire Hogan, Theodore Tae and June Kim•
Top U.S. health officials urged pregnant women not to use acetaminophen, the active ingredient in Tylenol, claiming it could cause autism, though studies have been inconclusive. Azeen Ghorayshi, a science reporter for The New York Times, explains.
Health
Autism by the numbers: Experts share reasons for the dramatic surge in diagnoses

NEWYou can now listen to Fox News articles!
Monday’s sweeping autism announcements have sparked deeper conversations about the widespread neurological disorder.
Health officials spoke during a press conference in Washington, D.C., about possible causes, vaccine guidance and the potential for a cancer drug to double as an autism therapy.
Autism diagnoses have been steadily rising in recent decades, according to the Centers for Disease Control and Prevention.
AUTISM SPECTRUM IN ADULTS HAS COMMONLY OVERLOOKED SYMPTOMS, EXPERTS WARN
“In the 1970s, autism was considered rare, perhaps 1 in 5,000 to 10,000 children,” Steven Quay, M.D., Ph.D., a physician-scientist and founder of Atossa Therapeutics in Seattle, Washington, told Fox News Digital.
In the year 2000, an estimated one in 150 children aged 8 had the disorder. By 2010, that number had risen to one in 68 — and by 2022, one in 31 children were diagnosed.
Autism diagnoses have been steadily rising in recent decades, according to the Centers for Disease Control and Prevention. (iStock)
“Autism is no longer an uncommon condition tucked away in psychiatric textbooks,” said Quay. “It is part of the daily fabric of schools, clinics and families everywhere.”
Dr. Aggie Papazyan, a Los Angeles-based psychologist specializing in autism spectrum disorder, noted that autism prevalence has also increased globally.
CANCER DRUG COULD DOUBLE AS AUTISM THERAPY, AND IS POISED FOR FDA APPROVAL
“These rates vary by region,” she told Fox News Digital. “In many places, especially in higher-income settings with more robust diagnostic and health resources, prevalence estimates have gone up.”
She added, “However, it’s important to note that how autism is measured makes a big difference.”
Awareness vs. epidemic
The CDC has noted that improved identification of autism could be part of the increase, but that other factors could also come into play.
Decades ago, many autistic people were “missed, misdiagnosed or labeled differently,” said Papazyan.
“There doesn’t seem to be a sudden surge in biological incidence.”
“Over time, as awareness has grown, diagnostic definitions expanded and screening became a bit more routine — so it’s not a surprise to see more autism diagnoses,” she said.
“The biggest misconception is that rising numbers mean autism itself is suddenly becoming more common,” the expert went on. “That’s scary to some people, but there’s no new autism ‘epidemic.’”

Experts say more funding is needed for early intervention programs, such as speech, occupational and behavioral therapies. (iStock)
Most of the increase, according to Papazyan, is due to earlier intervention, broader diagnostic criteria and improved access to services.
“There doesn’t seem to be a sudden surge in biological incidence,” she added. “There may still be a true rise, but it’s not as dramatic as many people want to think.”
Quay said it would be “naïve” to assume that the rise is due only to better detection, and said that environmental change also plays a role.
“Fifty years ago, many individuals on the spectrum were mislabeled — sometimes as intellectually disabled, sometimes as ‘eccentric’ or ‘odd,’ but I do not believe this accounts for the entire increase,” he said.

To counter the rising autism diagnoses, experts call for increasing awareness and acceptance while reducing stigma. (iStock)
“Environmental influences, from prenatal exposures to changes in maternal health to shifts in early childhood experiences, likely play some role.”
‘Urgent need’
To counter the rising autism diagnoses, Papazyan is calling for increasing awareness and acceptance while reducing stigma, as this affects how resources are allocated.
“Beyond that, we need to expand diagnostic and assessment services, especially in underserved communities, so that people are properly diagnosed and given the care they need,” she said.
Papazyan said more funding is also needed for early intervention programs, such as speech, occupational and behavioral therapies.
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The experts also agreed that support is needed for autistic people as they get older, including mental health services, financial assistance and life skills development.
“Interventions are needed that go beyond childhood, because autistic adults will spend most of their lives outside the school system, yet services for them are almost nonexistent,” said Quay.
“Fifty years ago, many individuals on the spectrum were mislabeled.”
Looking ahead, Papazyan predicts that autism prevalence will continue to increase over the next few years before it slows down and eventually hits a plateau.
Quay also expects that prevalence will continue to rise in the near term, largely due to improvements in detection and “societal willingness to diagnose.”
For more Health articles, visit www.foxnews.com/health
“Whether there is a biological plateau remains to be seen,” he said. “If environmental contributors are identified and mitigated, we could see stabilization.”
Health
Who Makes Vaccine Policy Decisions in RFK Jr.’s Health Department?

For decades, as an activist, Robert F. Kennedy Jr. resisted the scientific consensus that vaccines are safe and necessary to prevent serious disease. Now at the helm of the nation’s health department, he has begun to put his extreme views into practice, ousting veteran scientists and installing allies across the nation’s health agencies to enact major shifts in vaccine policy.
Some of Mr. Kennedy’s hires are activists who have worked for years alongside him. Others are scientists who say they broadly support vaccines but publicly criticized Covid shots or mandates during the pandemic. Many of these scientists have begun to question the safety or value of other shots, reflecting the views of Mr. Kennedy. The following account is based on previous statements made by these officials and on interviews with current and former health agency leaders.
F.D.A. chief medical and scientific officer
Critical of Covid boosters and shots for healthy kids
F.D.A. commissioner
Skeptical of certain vaccines
Dr. Vinay Prasad
Dr. Marty Makary
The agency’s new vaccine lead and chief medical officer, Dr. Vinay Prasad, has called himself an “extreme pro-vaccine person,” and Dr. Marty Makary, the agency’s commissioner, said last week that “we believe in vaccines.”
But the two officials, who sharply criticized vaccine mandates as academic researchers during the pandemic, have expressed doubts about the safety and necessity of Covid boosters for healthy children and adults. This summer, Dr. Prasad overrode some agency scientists who favored widespread access to Covid shots, narrowing the vaccine’s eligibility to those 65 and older and to younger people with underlying medical conditions.
Last week, Dr. Makary echoed the views of Mr. Kennedy when he publicly questioned the longstanding recommendation to give the hepatitis B vaccine at birth. That shot is credited with nearly eliminating the transmission of the disease from mother to infant.
Dr. Prasad replaced a veteran at the agency, Dr. Peter Marks, who resigned in March and said that Mr. Kennedy’s aggressive stance on vaccines posed a danger to the public.
In June, Mr. Kennedy fired all 17 members of a powerful C.D.C. expert panel, the Advisory Committee on Immunization Practices. Insurance companies and government programs like Medicaid are required to cover the vaccinations that the panel recommends.
Mr. Kennedy handpicked eight new members that month, half of whom had expressed skepticism of vaccines at some point. (One has since stepped down.) Others have little expertise in immunology or vaccines.
On Monday, Mr. Kennedy appointed five more members, just days before the group meets to review recommendations for multiple vaccines. Some of the newly selected members have been critical of Covid vaccines or vaccine mandates.
Dr. Robert Malone is a controversial figure. He performed early experiments using mRNA in the 1980s but gained notoriety during the pandemic for claiming that Covid vaccines were unsafe, contradicting volumes of studies.
Martin Kulldorff, a biostatistician, has been generally supportive of vaccines but opposed Covid vaccination for children and vaccine mandates. Vicky Pebsworth, a nurse with a doctorate in public health, serves on the board of the National Vaccine Information Center, a nonprofit that disseminates misinformation about the risks of vaccination.
Dr. Malone and Dr. Kulldorff have served as paid expert witnesses in legal cases against vaccine makers. Dr. Pebsworth claimed in a lawsuit that a survey of families of unvaccinated children supported a hypothesis that a rise in the number of recommended childhood vaccines explained an epidemic of chronic disease.
Another panel member, Retsef Levi, is a management and health analytics expert at the Massachusetts Institute of Technology. He has been critical of a variety of vaccines and has called for Covid vaccines to be pulled from the market.
Dr. Evelyn Griffin, an obstetrician and gynecologist, questioned the safety and effectiveness of Covid vaccines in a hearing in the Louisiana House of Representatives in 2021. Dr. Kirk Milhoan, a pediatric cardiologist, questioned the safety and effectiveness of Covid vaccines at a 2024 event led by Representative Marjorie Taylor Greene, Republican of Georgia. Catherine M. Stein is an epidemiology professor who in 2022 called for an end to Covid vaccine mandates at universities.
Dr. Cody Meissner is a professor of pediatrics who opposed vaccine mandates and has questioned the ongoing need for Covid vaccines for children and pregnant women. He previously served on the advisory committee and is widely considered to be the most qualified member.
The others are not known to have spoken out against vaccines. They are Dr. Joseph R. Hibbeln, a nutritional neuroscientist; Dr. James Pagano, an emergency medicine physician; Hillary Blackburn, a pharmacist; and Dr. Raymond Pollak, a surgeon and transplant specialist.
The C.D.C. director has the power to accept or reject the immunization committee’s recommendations. The current acting director is Mr. Kennedy’s deputy at the Department of Health and Human Services, Jim O’Neill, a former biotechnology executive. The previous director, Susan Monarez, said she was forced out because she would not agree to accept the newly re-formed committee’s recommendations.
A special adviser to the C.D.C. director, Stuart Burns, is a critical player driving the health secretary’s agenda at the agency. Mr. Burns has been quietly working to remake the immunization committee and its agenda.
Mr. Burns is not a scientist but he worked for decades as a staff member for Republican congressmen known for their vaccine skepticism. One is Dr. Dave Weldon, a former representative from Florida who was also Mr. Kennedy’s original choice for C.D.C. director. The White House withdrew Dr. Weldon’s nomination just hours before his confirmation hearing because some Senate Republicans were concerned about his stance on vaccines.
Mr. Burns works closely with three other Kennedy hires who serve H.H.S. but also work closely with the C.D.C. Dr. Reyn Archer is a former Texas health commissioner who has questioned the safety and value of the Covid vaccine on social media. He serves as a liaison between the health secretary’s office and the C.D.C., and has been helping Mr. Burns to develop and guide the immunization committee.
David Geier is a steadfast figure in the anti-vaccine movement who has spent more than 20 years trying to establish a link between vaccines and autism, despite scientific consensus that there is none. Mr. Geier, who is listed as a senior data analyst in the H.H.S. directory, was given access to federal data on post-vaccination side effects and is using it to continue his studies on autism.
Lyn Redwood is a nurse practitioner and the former head of Children’s Health Defense, the anti-vaccine group founded by Mr. Kennedy. Since the early 2000s, Ms. Redwood has criticized the use of mercury as a preservative in vaccines. She has said she believes the ingredient is linked to her son’s autism.
Now listed as an expert at H.H.S., Ms. Redwood gave a presentation in June to the immunization committee, a role usually reserved for C.D.C. scientists. She said that the mercury preservative in vaccines, known as thimerosal, was toxic to children, even though dozens of studies have shown it is harmless in this form. The panel later voted to stop recommending the already limited number of flu vaccines that contained the preservative.
Principal deputy director of the N.I.H.
Skeptical of certain vaccines
N.I.H. director
Critical of Covid vaccine mandates
Dr. Matthew Memoli
Dr. Jay Bhattacharya
Dr. Matthew Memoli is a veteran infectious disease scientist at the National Institutes of Health who now serves as its principal deputy director. As a senior researcher under Dr. Anthony Fauci during the pandemic, Dr. Memoli opposed Covid vaccine mandates and declined to get a shot himself.
Since becoming a leader of the research agency, Dr. Memoli has downplayed the value of vaccines for certain respiratory diseases, according to the whistle-blower complaints of two prominent scientists.
Dr. Jay Bhattacharya, the N.I.H director, sharply criticized vaccine mandates as an academic researcher during the pandemic. He co-wrote an anti-lockdown treatise in 2020 with Dr. Kulldorff, one of Mr. Kennedy’s selections for the C.D.C. immunization committee.
During his confirmation hearing in March, Dr. Bhattacharya reiterated his support for childhood vaccinations for diseases like measles. He also said he was “convinced” vaccines did not cause autism, even as he urged more research on the question, which scientists say has long been settled.
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