PSI Chairman Johnson Releases Report; Will Hold Hearing on Federal Health Agencies’ Failure to Warn About the Risk of Myocarditis Following COVID-19 Vaccination
WASHINGTON – Today, U.S. Sen. Ron Johnson (R-Wis.), chairman of the Permanent Subcommittee on Investigations (“PSI” or “Subcommittee”), will hold a hearing entitled, “The Corruption of Science and Federal Health Agencies: How Health Officials Downplayed and Hid Myocarditis and Other Adverse Events Associated with the COVID-19 Vaccines.” In conjunction with the hearing, the chairman released an interim Majority Staff Report, along with more than 2,400 pages of records, detailing the failure of federal health agencies to properly warn the public of the risks of myocarditis and related heart inflammation conditions following mRNA COVID-19 vaccination. The report, which follows Chairman Johnson’s Jan. 28, 2025 subpoena to the Department of Health and Human Services (“HHS”), reveals how federal health officials who were aware of reports of heart inflammation conditions associated with mRNA COVID-19 vaccines delayed notifying the public while downplaying the risks.
Records produced pursuant to the subpoena reveal the following: in the first half of 2021, federal health officials had ample evidence of myocarditis and related heart inflammation conditions occurring in young adults who received mRNA COVID-19 vaccines. Although a number of these records were previously made available to the public through the Freedom of Information Act (“FOIA”), the Biden administration’s heavy redactions prevented a full understanding of what federal health officials knew and what actions they took.
As detailed in the report and records Chairman Johnson released, beginning in February 2021, federal health officials were put on notice by counterparts in Israel of individuals experiencing myocarditis and related heart inflammation conditions after receiving mRNA COVID-19 vaccination. Over the next three months, federal health officials continued to receive information on cases of heart inflammation following mRNA COVID-19 vaccination. By mid-May 2021, Centers for Disease Control and Prevention (“CDC”) officials were drafting a formal notification for health care providers and other officials.
Records indicate that while health officials were drafting the notification, a key vaccine safety monitoring system, VAERS, began showing a safety signal for a heart inflammation condition in young adults who had received an mRNA COVID-19 vaccine. Within days of the safety signal, the top ranking official at the Food and Drug Administration (“FDA”), then-Acting Commissioner Janet Woodcock, pushed back on the CDC’s plan to formally notify healthcare providers, ultimately resulting in the formal notification being rejected in favor of a posting on CDC’s website.
The report builds on the work of many individuals who fought tirelessly to obtain records through the FOIA process under the Biden administration. The chairman credits Brenda Baletti, Ed Berkovich, Brian Hooker, Amy Kelly, Zachary Stieber, Naomi Wolf, and many others who worked persistently to expose the truth about the association of myocarditis with the COVID-19 vaccines.
With the release of the interim report and the corresponding subpoenaed documents produced by the Trump administration, the public will be able to access a more complete record of the Biden administration’s failure to warn the public about the health risks of COVID-19 vaccines without heavy FOIA redactions.
Key findings from the report include:
- Despite their awareness of the risks, U.S. health officials downplayed the risks of myocarditis and associated heart inflammation conditions after receiving an mRNA COVID-19 vaccine.
- U.S. health officials delayed for months alerting the public, and ultimately rejected a formal notification to health care providers about the risks to young people of myocarditis and associated heart inflammation conditions following receipt of an mRNA COVID-19 vaccine.
- U.S. health officials were made aware by at least early 2021 that some of their vaccine safety monitoring systems may not have been capturing all cases of myocarditis and associated heart inflammation following receipt of an mRNA COVID-19 vaccine.
The hearing will be live streamed beginning at 2:00pm EST here.
The interim PSI Majority Staff report can be found here.
The records, which at the request of HHS contain minimal redactions for Personally Identifiable Information, are linked below:
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