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Wednesday, 01 April 2020 06:53

Johnson & Johnson using aborted babies for COVID-19 vaccine

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Johnson & Johnson using aborted babies for COVID-19 vaccine Photo by Polina Tankilevitch from Pexels

(Clearwater, FL) For the second time in less than a week, Children of God for Life is calling out the pharmaceutical industry for the use of aborted fetal cell lines in potential Covid-19 vaccines.

On March 25th, the organization exposed Moderna’s use of the aborted fetal cell line HEK 293 and the morally produced version by Sanofi Pasteur. This time it’s Janssen Pharmaceutical, owned by Johnson and Johnson, that is using their PER C6 Ad5 technology, derived from an aborted baby’s retinal tissue. Dr. Alex van der Eb revealed the information on this abortion at FDA hearings in 2001:

“So I isolated retina from a fetus, from a healthy fetus as far as could be seen, of 18 weeks old. There was nothing special with a family history or the pregnancy was completely normal up to the 18 weeks, and it turned out to be a socially indicated abortus – abortus provocatus, and that was simply because the woman wanted to get rid of the fetus… what was written down was unknown father, and that was, in fact, the reason why the abortion was requested.”

Adding insult to injury, Dr. van der Eb went on to admit: “PER C6 was made just for pharmaceutical manufacturing of adenovirus vectors… And then pharmaceutical industry standard. I realize that this sounds a bit commercial, but PER C6 were made for that particular purpose.”

Not only are there moral problems with using aborted fetal cells, but the PER C6 Ad5 technology also has safety concerns that have been raised with the FDA as well.

“Residual DNA in vaccines derived from tumorigenic cells, including those transformed by Ad5, can pose potential risks to the vaccine recipient in two respects: oncogenicity and infectivity. Each of these biological properties must be considered and evaluated for each cell substrate.”

Vinnedge noted there is not one FDA-approved vaccine in the US using this cell line, though several did take interest when it was announced in 2001. One of those companies was Merck who tried the cell line in a new HIV vaccine but ended the project in 2007 when the vaccine proved to be ineffective.

“This is about as irresponsible as the industry can get”, stated Debi Vinnedge, Executive Director of Children of God for Life. “We have a worldwide pandemic where millions of people are in need of treatment and prevention of disease. Yet Johnson and Johnson is choosing to produce a vaccine that a large number of people of good conscience will refuse due to the aborted fetal cells!”

In their own Code of Business Conduct, Johnson & Johnson states that “We believe acting ethically and responsibly is not only the right thing to do, but also the right thing to do for our business. Our Johnson & Johnson Code of Business Conduct ensures that we hold ourselves and how we do business to a high standard, allowing us to fulfill our obligations to the many stakeholders we serve.”

But their use of aborted fetal material in consumer medicines is far from the high ethical standards or concern for their customers and stakeholders whom they are claiming to serve. The irony of what they are doing in using aborted fetal cell lines is not lost to the casual observer.

“How despicable that a company whose success was largely acquired from its’ products for living babies is trying to capitalize on the remains of a deliberately murdered one”, she added.

To voice your concerns, contact:
Johnson & Johnson
Alex Gorsky, CEO
One Johnson & Johnson Plaza
New Brunswick, New Jersey 08933
(732) 524-0400


PER C6 cell line – FDA hearings:

Ad5 Safety Concerns:

Merck HiV failure:

Debi Vinnedge

Debi Vinnedge is the Executive Director of Children of God for Life, a non-profit, pro-life organization focused on the bioethic issues of human cloning, embryonic and fetal tissue research. In addition she serves as a member of the Board at Sound Choice Pharmaceutical Institute and her organization is an official member of the American Life League Associates program.

Ms Vinnedge is a nationally recognized author and speaker and has provided written testimony for Congressional hearings on embryonic stem cell research. She introduced the Fair Labeling and Informed Consent Act to members of the US House and Senate, legislation that protects religious rights, moral conscience and requires informed consent on medical products using aborted fetal or embryonic materials.

Ms Vinnedge is considered the foremost authority on the use of aborted fetal cell lines in medical products and vaccines. Her organization’s Campaign for Ethical Vaccines has gained the backing of over 638,000 supporters nationwide including numerous medical professionals, pro-life organizations, religious and political groups.