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  "description": "Insider accounts, leaked memos and Congressional scrutiny reveal what happened behind closed doors at the FDA after reports of paediatric deaths following Covid vaccination.",
  "path": "/reproduced-with-permission-duplicate-copy-11/",
  "publishedAt": "2026-05-26T00:30:04.000Z",
  "site": "https://goodoil.news",
  "tags": [
    "Maryanne Demasi",
    "interview",
    "leaked",
    "Korea",
    "Israel",
    "internal memo",
    "wrote",
    "backlash",
    "reported",
    "ACIP discussions",
    "confirmed",
    "fired",
    "MD Reports"
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  "textContent": "Maryanne Demasi\n_Maryanne Demasi PhD is an investigative journalist who writes for online media and top tiered medical journals. For over a decade, she was a TV presenter for the Australian Broadcasting Corporation._\n\nIn September 2025, then-US Food and Drug Administration (FDA) Commissioner Dr Marty Makary publicly acknowledged that the agency was investigating reports of child deaths following Covid-19 vaccination.\n\n“We do know at the FDA… that there had been children who have died from the COVID vaccine,” Makary said during a CNN interview.\n\nBy that stage, however, a fierce internal dispute had already emerged inside the FDA over what investigators believed the evidence showed – and whether the public should ever see the full findings.\n\n“It really did feel like there was some sort of cover-up going on about the Covid-19 vaccines,” said one individual familiar with the discussions.\n\n_MD Reports_ spoke with several current/former agency officials, advisers, and individuals briefed on the discussions, all of whom requested anonymity because they were not authorised to publicly discuss internal FDA deliberations.\n\nAt the centre of the controversy was an internal FDA review led by Dr Tracy Beth Høeg, a physician-scientist who was working as a senior scientist inside the FDA’s vaccine division at the time.\n\nFDA officials examined roughly 96 paediatric death reports submitted to the Vaccine Adverse Event Reporting System (VAERS), the government database used to detect potential vaccine-related adverse events.\n\nThe review included medical records, autopsy reports, pathology findings, and follow-up investigations conducted by agency staff.\n\nAbout 25 deaths following Covid vaccination were ultimately considered serious enough for high-level internal discussion inside the agency.\n\nThe findings were expected to be presented at a September 2025 meeting of the CDC’s Advisory Committee on Immunisation Practices (ACIP), the federal panel that shapes US vaccine recommendations.\n\nBut before that could happen, details of the review leaked to the _New York Times_ and the _Washington Post_.\n\nHøeg quickly became the focus of intense media scrutiny and criticism from vaccine advocates and unnamed FDA officials who argued she was relying too heavily on VAERS reports and overstating preliminary findings.\n\nPeople familiar with the fallout said some FDA staff strongly objected to Høeg’s methods and conclusions and allegedly sought to undermine her credibility by leaking details of the review.\n\nThe leak effectively ended plans for a public ACIP discussion and deepened divisions within the FDA over how the findings should be handled.\n\nSome officials believed the findings warranted stronger warnings and greater transparency. Others feared public acknowledgement of vaccine-linked child deaths would damage confidence in the Covid vaccines.\n\n“We know that there are these deaths that are due to the vaccine,” said one source, referring to myocarditis cases and published reports from countries including Korea and Israel.\n\nThe controversy intensified after then-FDA vaccine chief Dr Vinay Prasad ordered additional investigation into the deaths identified in Høeg’s review.\n\nMonths later, another leak brought the issue back into public view.\n\nIn November 2025, an internal memo circulated by Prasad became public. In it, Prasad acknowledged that “at least 10” children had died “after and because of receiving Covid-19 vaccination”.\n\nHe described the findings as “a profound revelation”.\n\n“Covid-19 vaccines did result in the death of children,” Prasad wrote. “Dr Hoeg was correct in her assessment.”\n\nThe memo triggered another round of backlash from media outlets and vaccine advocates, many of whom accused Prasad of overstating the evidence before the agency’s analysis had been finalised.\n\n_Inside Medicine_ reported on a Dec 5 memo about a subsequent FDA analysis using a World Health Organization causality framework, which classified **_zero_** deaths as “certain”, two as “probable/likely”, and five as “possible.”\n\nBut individuals involved in the discussions said pressure steadily mounted inside the agency to “downgrade” the findings with each successive review.\n\n“It seemed like there was a lot of pressure to keep decreasing the number of deaths,” said one source.\n\n“It does seem like they tortured the data to get something that was more palatable.”\n\nAt the same time, tensions were also growing around another unresolved issue inside the FDA – residual DNA contamination in Covid mRNA vaccines.\n\nThe issue surfaced repeatedly during ACIP discussions throughout 2025, with some advisory group members seeking additional information from the FDA about DNA levels and biodistribution studies involving lipid nanoparticles.\n\nAccording to individuals familiar with the discussions, those requests were repeatedly delayed.\n\nOne individual identified Dr David C Kaslow, director of the FDA’s Office of Vaccines Research and Review (OVRR), as the official responsible for liaising with ACIP on the issue.\n\nAnother person involved in the discussions described Kaslow as the person “stonewalling” the issue of DNA contamination.\n\nDr David C Kaslow, ****Director of the Office of Vaccines Research and Review (OVRR) in the Center for Biologics Evaluation and Research (CBER)**** ,\n\nThe controversy has since drawn Congressional scrutiny.\n\nIn May 2026, Senator Ron Johnson wrote to Health Secretary Robert F Kennedy Jr referencing an FDA memorandum examining paediatric deaths following Covid vaccination.\n\nJohnson said the documents raised concerns about a potential “coverup” of vaccine safety risks.\n\nThe letter confirmed that FDA officials reviewed 96 paediatric deaths following vaccination and ultimately classified seven cases as either “possibly” or “probably” related to Covid vaccination.\n\nIt also acknowledged that fatal myocarditis cases represented “new safety information” and documented discussions about revised vaccine warning labels.\n\nBy then, the internal dispute at the FDA had expanded beyond the deaths themselves and into a broader fight over vaccine safety warnings.\n\nHøeg later delivered an internal presentation arguing that Covid mRNA vaccines warranted a black box warning – the FDA’s strongest warning reserved for products associated with serious injury or death.\n\nThe proposed warning would have explicitly acknowledged the risk of death in children.\n\n“If a vaccine has potential to cause death to children, I think it should be on the label,” said one source familiar with the discussions.\n\nHøeg’s proposal was ultimately rejected by the agency.\n\nIn December 2025, Makary publicly confirmed that the FDA had declined an internal recommendation for a black box warning on Covid mRNA vaccines.\n\nMakary argued that earlier safety concerns emerged during the initial multi-dose rollout and might not apply to annual vaccination schedules.\n\nAccording to individuals familiar with the discussions, Høeg’s persistent probing of Covid vaccine safety issues increasingly isolated her inside the agency.\n\nHer eventual transfer out of the vaccine division and into the FDA’s drug division, CDER, effectively ended her involvement in those investigations.\n\nJust recently, Høeg was fired from the agency after refusing to resign from her position.\n\nTo this day, the FDA has never publicly released the full paediatric death review examining 96 VAERS reports of child deaths following Covid vaccination, nor the multiple revised versions of the agency’s subsequent analyses.\n\n“Why do we collect these VAERS reports if we’re not going to explain to the public what we find?” said one source.\n\nNow, months after the internal disputes first erupted, the FDA continues to face questions about what officials knew, when they knew it, and why the agency failed to promptly release its investigations into paediatric deaths following Covid vaccination.\n\nThis article was originally published by MD Reports.",
  "title": "Inside the FDA’s ‘Cover-Up’ Over Child Deaths",
  "updatedAt": "2026-05-26T00:30:03.750Z"
}