October 22, 2023 Steve Kirsh Substack

Breaking: You can now sue the mRNA COVID vaccine manufacturers for damages and the FDA is required to take the COVID vaccines off the market. Why? Adulteration. The plasmid bioactive contaminant sequences were NOT pointed out to the regulatory authorities. It’s considered adulteration. I just got off the phone with Professor Byram Bridle and Dr. Robert Malone on this. 

Michigan remdesivir case is very important precedent here proving liability shield falls when there is undisclosed contamination of active ingredients. 

I’m doing a video interview with Byram and with Kevin tomorrow on this topic. 

The FDA is now at a crossroads. Either they admit that they knew about the plasma contamination, and failed to disclose that to the public and to the outside committees, or they can claim that they didn’t know about it in which case Pfizer is liable. But we have the Pfizer documents that were given to the FDA so we know what the FDA got. And I seriously doubt there’s any disclosure of SV40 contamination. That means we have an adulterated vaccine and the FDA has to remove it from the market until the adulteration is fixed. If the FDA doesn’t do that, they should face criminal prosecution for endangering the public, and not following the law. 

Here’s the Michigan story for those who asked showing when there is contamination, there is no immunity. It makes sense. Otherwise, they can add arsenic into the vaccines and not be liable.

All the COVID production vials are contaminated AFAIK. From both Moderna and Pfizer. 

I just message Dr. Naomi Wolf re: Pfizer docs. She wasn’t aware of any mention of SV40 in the Pfizer docs they gave the FDA (but she will check further).

So Pfizer has a VERY BIG problem. 

I just got off the phone with attorney Warner Mendenhall. He confirmed I wrote is accurate and the litigation floodgates are now open.

Here is a list of 90 lawyers that you can contact if you want to sue the vaccine manufacturers: airtable.com/appGIUGnttjzsc

The SV40 promoter is found in all the vials and it was in the gene sequence that was provided to the regulators. There is no mistake. The problem was that neither drug company ever pointed it out to the regulators. It’s an unapproved contaminant that doesn’t meet the standards set. So the regulators are off the hook. But if the regulators don’t take action, then they dig themselves into a very deep hole. The law requires the FDA to stop the vaccine. 

Robert Malone @RWMaloneMD just messaged me: “Yes I think that this DNA adulteration issue could be the wedge we have been looking for. Use of a plasmid with SV40 sequences as the template for manufacturing the pseudo-mRNA is, at a minimum, reckless and I can see no logical justification” 

It does appear that Biden and most all of the US lawmakers are supporting the drug companies. That’s what they’re paid to do.

Why do I say that? The adulteration has been known since April 2023 and nobody has called for an investigation. Not even after Health Canada confirmed it. They didn’t even ask for an investigation!!

Also, not a single mainstream doctor, who was promoting the vaccine has called for the proper testing to be done as far as I know. The brainwashing and intimidation here is stunning. Everyone should be calling for this to be taken extremely seriously.

I can tell you that all of MY scientific friends want to see this work done ASAP.

If it is discovered that this integrates into your DNA, no one will want to take it willingly.

Our government will then need to mandate it to get people to comply, just like they did before.

If people in government were interested in science and your health, they would have been hammering the CDC and the FDA asking why this was never investigated when it was first discovered.

It will be interesting to see what they do now, won’t it?