Blood banks routinely screen donations for recognised infectious threats. But they are not screening for vaccine-derived spike protein, plasmid DNA or other harmful vaccine-related constituents.
So, researchers set out to investigate the possible effects blood donations from covid-vaccinated people were having on recipients. Yesterday they published a study on a preprint server describing what they found.
The study identified nine unvaccinated blood transfusion recipients who experienced serious complications, including blood clots, heart damage, multi-organ failure and death.
“This study suggests that blood donated by covid-19-vaccinated individuals may contain biologically active vaccine-derived constituents that could cause adverse clinical outcomes,” the authors wrote.
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Two New Studies Raise Alarm Over Potential COVID-19 “Vaccine” Contamination of the Blood Supply
By Nicolas Hulscher, as published by Focal Points on 21 August 2026
A newly published two-part scientific study raises major alarms about an issue that has received remarkably little scrutiny: What happens when blood from covid-19-vaccinated donors is transfused into another person?
Blood banks routinely screen donations for recognised infectious threats. Yet the current blood supply is not routinely screened for vaccine-derived mRNA, spike protein, plasmid DNA, amyloid, fibrin-microclot complexes, or other relevant vaccine-associated constituents.
Our newly published two-part series investigates this blind spot from two complementary directions. The two studies were authored by James A. Thorp, MD; Claire Rogers, MSPAS, PA-C; R. Clinton Ohlers, PhD; M. Nathaniel Mead, PhD; Nicolas Hulscher, MPH (myself); Kirstin Cosgrove, CCRA; Sierra Hamm, RN; David Speicher, PhD; and Steven Hatfill, MD, M Med.
Part I: Serious Post-Transfusion Complications in Nine Unvaccinated Patients
Part I presents a retrospective, hypothesis-generating case series of nine people who had not received a covid-19 vaccine and subsequently experienced serious medical events after receiving blood transfusions.
Reported complications included thromboembolic disease, progressive clotting disorders, myocarditis, pericardial disease, disseminated intravascular coagulation, multi-organ system failure and death.
We concluded that these cases, together with the existing literature, raise sufficient concern to warrant direct investigation of whether biologically active vaccine-derived constituents may be present in donated blood:
This study suggests that blood donated by covid-19-vaccinated individuals may contain biologically active vaccine-derived constituents that could cause adverse clinical outcomes. The case reports and cited studies identify questions that warrant further investigation. All the pathogenic components of the covid-19 vaccine or byproducts from it have been found in several studies to be circulating in the blood of vaccinated donors. Healthcare providers must honour the ethical principles of patient autonomy and non-maleficence and support patients’ requests for autologous and directed designated donor blood. Screening blood donations for the presence of spike protein, amyloid, fibrin-microclot complexes, vaccine-derived mRNA and plasmid DNA using quantitative assays and PCR-based methods should be considered for further evaluation by relevant public health and regulatory authorities, including the CDC and FDA.
Thorp, J. A., Rogers, C., Ohlers, R. C., Mead, M. N., Hulscher, N., Cosgrove, K., Hamm, S., Speicher, D., & Hatfill, S. (2026). Potential Implications of COVID-19 Vaccination for Blood Donation: A Retrospective Case Series and Literature Review—Part I of II. Zenodo. https://doi.org/10.5281/zenodo.22036329
Part II: Extraordinary Blood, Clotting, and Neurological Safety Signals
Part II expands the investigation to the CDC/FDA Vaccine Adverse Event Reporting System (“VAERS”), analysing reports from 1 January 1990 through to 26 June 2026 and comparing covid-19 vaccines with influenza vaccines, DPT-containing vaccines, and all non-covid vaccines combined.
The analysis identified statistically significant safety signals across every investigated endpoint, including reported rate ratios reaching:
- Haemorrhage: up to 101-fold
- Haemorrhage in pregnancy: up to 108-fold
- Blood transfusion: up to 62-fold
- Post-transfusion complications: up to 30-fold
- Hypercoagulable biomarkers: up to 452-fold
- Thrombotic events: up to 1,221-fold
- Parkinson’s disease: up to 282-fold
- Creutzfeldt-Jakob disease: up to 1,333-fold
- Prion disease: 60-fold
These signals are particularly important because they overlap with many of the same clinical patterns observed in Part I, including thrombosis, haemorrhage, DIC [disseminated intravascular coagulation] and multi-organ dysfunction.
Part I identifies a series of serious post-transfusion events that demand investigation. Part II identifies striking pharmacovigilance signals involving many of the same biological systems, particularly clotting, haemorrhage, transfusion complications and multi-organ dysfunction.
To preserve global blood-supply integrity, regulatory frameworks should move rapidly to implement direct quantitative spike-protein screening and high-sensitivity digital PCR testing for vaccine-derived genetic material across donor networks, while also investigating whether these constituents remain biologically active after donation, storage, processing and transfusion.
About the Author
Nicolas Hulscher, Master of Public Health (“MPH”), is an epidemiologist and Administrator at the McCullough Foundation, which publishes articles on a Substack page titled ‘Focal Points’.
Hulscher is known for his research on adverse events following covid vaccination, particularly focusing on myocarditis and other post-acute sequelae. He has been the lead author on several covid vaccination studies and a contributor to others. He has also co-authored research on the proximal origin of highly pathogenic avian influenza H5N1.
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