Wed Dec 10 17:16:19 UTC 2025: Summary:

The US Food and Drug Administration (FDA), under the direction of Health Secretary Robert F. Kennedy Jr. (a known vaccine skeptic), is conducting a broad investigation into deaths potentially linked to COVID-19 vaccines. The investigation, initially focused on child deaths, became controversial after a leaked memo claimed a link between COVID vaccines and infant deaths without evidence. Experts are concerned about the investigation’s potential bias due to Kennedy’s history of spreading misinformation about vaccines, despite evidence of the vaccines’ safety and efficacy.

News Article:

FDA Launches Broad Investigation into COVID Vaccine Deaths Under Vaccine-Skeptic Health Secretary

Washington, DC – The U.S. Food and Drug Administration (FDA) is facing scrutiny as it conducts a wide-ranging investigation into deaths potentially linked to COVID-19 vaccines. The probe, announced on Tuesday by a spokesperson for Health Secretary Robert F. Kennedy Jr., has sparked controversy due to Kennedy’s well-documented history of vaccine skepticism and the dissemination of misinformation.

The investigation, initially focused on child deaths, was further inflamed by the leak of an internal FDA memo in late November. The memo, attributed to a senior FDA official, claimed a connection between COVID vaccines and at least 10 infant deaths, though it lacked supporting evidence.

The move comes amidst a significant overhaul of vaccine policy under the Trump administration, raising concerns within the medical community. Experts are particularly worried about the potential for bias given Kennedy’s past statements, including a 2023 claim that COVID vaccines were “deadly” and an unsubstantiated allegation that the virus was ethnically targeted.

While acknowledging the possibility of rare severe side effects, global health authorities have overwhelmingly supported the safety and efficacy of COVID vaccines, demonstrating their overall benefit for most age groups. It remains unclear what methods, data, or timeline the FDA will use to conduct its investigation.

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