Pfizer and Moderna guilty of breaches of 21 U.S. Code § 351 - Adulterated drugs and devices – and - 21 U.S. Code § 360d - Performance standards – maybe 17 trillion in compensation owed to Americans

Ten times that globally - reparations needed - but who has that kind of money? A long term health plan is needed to cure and treat those maimed - to reduce the bill

In one of my first SubStack posts here

Covid19 remedies - the legal ones - by Peter Halligan (substack.com)

Followed up here:

How many breaches of Section 21 US Code have there been - let us count the ways (substack.com)

I referenced a few clauses:

Here is are the section headings from Code 351

“A drug or device shall be deemed to be adulterated—

(a)Poisonous, insanitary, etc., ingredients; adequate controls in manufacture

(b)Strength, quality, or purity differing from official compendium

(c)Misrepresentation of strength, etc., where drug is unrecognized in compendium

(d)Mixture with or substitution of another substance

(e)Devices not in conformity with performance standards

(f)Certain class III devices

(g)Banned devices

(h)Manufacture, packing, storage, or installation of device not in conformity with applicable requirements or conditions

(i)Failure to comply with requirements under which device was exempted for investigational use

(j)Delayed, denied, or limited inspection; refusal to permit entry or inspection

Note also that the FDA had found Moderna to be in breach of manufacturing codes as described I an article a year ago  in an article by Hadley Rees way back in September 2022.

(100) Recall of Moderna C19 Injections? - by Peter Halligan (substack.com)

Referenced more fully for the unpaid subscriber here:

(100) Recall of Moderna C19 Injections? - by Peter Halligan (substack.com)

“OBSERVATION 1

Your firm failed to thoroughly investigate any unexplained discrepancy or failure of a batch or any of its components to meet any of its specifications, whether or not the batch has already been distributed.

OBSERVATION 3

Control procedures are not established which monitor the output and validate the performance of those manufacturing processes that may be responsible for causing variability in characteristics of the in-process material and the drug product.

OBSERVATION 4

Acceptance criteria for the sampling and testing conducted by the quality control unit is not adequate to ensure that batches of the drug product meet appropriate statistical quality control criteria as a condition for their approval and release.”

So, the FDA knew about poor manufacturing a long long time ago.

Now that Health Canada has confirmed the contents of the vials were adulterated with segments of the SV40 sequence  that were NOT disclosed to Health Canada, it follows that regulators globally have also been so deceived. This does not mean that there are no other contaminants that led to deaths and injuries – endotoxins, pseudo uridine, different size of spike protein manufactured by the immune system compared to the size of the spike protein in the infection, PEG coating, lipids etc. It refers ONLY to the SV40 contaminant concealed from regulators.

What goes for Canada goes for global health regulators. Of course, it reveals their guilt in failing to monitor the quality of conformance and compliance of doses with those of the clinical trials, which already indicated more harm than good in terms of severe (life altering), serious (life threatening) and mortality events.

The compliance failures are failures of the regulators who should have been extra vigilant in what was an EXPERIMENTAL process manufactured by companies with ZERO EXPERIENCE of manufacturing such experimental products AND for which such experimental products had never been used in a public health setting, let alone proven successful in any other settings, small or large.

The response from Health Canada is covered in this SubStack and indicates how damning Health Canada:

(100) Explosive Story: Health Canada Admits Pfizer Misrepresented Their COVID-19 Shot (substack.com)

Referencing this Epoch Times article:

EXCLUSIVE: Health Canada Confirms Undisclosed Presence of DNA Sequence in Pfizer Shot | The Epoch Times

Check out these quotes directly from Health Canada that apply to every health regulator in the world – (does not include any other contaminants!).

“Health Canada expects sponsors to identify any biologically functional DNA sequences within a plasmid (such as an SV40 enhancer) at the time of submission"

"Although the full DNA sequence of the Pfizer plasmid was provided at the time of initial filing, the sponsor did not specifically identify the SV40 sequence."

“it was possible for Health Canada to confirm the presence of the enhancer based on the plasmid DNA sequence submitted by Pfizer against the published SV40 enhancer sequence."

Of note is that last statement – Health Canada has the capacity to detect the presence of the enhancer..” – this probably means it has always had such a capacity and either did not engage in the use of such capacity or ignored it. The same applies to every other health regulator globally and it also applies to the pretender to the throne of global health regulations – THE WORLD HEALTH ORGANIZATION.

Health regulators are jointly and severally charged with monitoring quality and compliance and collaborating with each other to ensure these features.

They failed – and as a result, despite all the conventions and communications amongst and between themselves over decades, they have proven to be useless and ineffectual in precenting what should have been a blatantly obvious need to be extra vigilant.

And this is what G20 leaders, the WHO and a bunch of unqualified bureaucrats are attempting to make “de rigueur” via changes to International Health Regulations and a new Pandemic Treaty – via “silence = consent”.

Now, I am not a lawyer, but I would imagine that the way is now clear for, if not criminal, then civil damages to be awarded to each individual killed or maimed by the C19 mRNA injections of Moderna and Pfizer/BioNTech.

I guess that a class action suit worth five million for deaths (possibly more than 700,000 in the US alone) and an average claim of around 2 million for serious - life threatening) harms - (around 3.5 million) and 1 million for severe (life altering) events (around 7 million). Those numbers are based on a URF of around 40 and 670 million mRNA doses administered in the US, plus the latest VAERS deaths combined with the incidence of harms from the Pfizer Phase 3 clinical trials here (pages 11 and 12):

The COVID-19 Inoculations - More Harm Than Good FINAL Video & Print (canadiancovidcarealliance.org)

700,000 times 5 million = 3.5 trillion bucks

3.5 million times 2 million = 7 trillion bucks

7 million 1 million = 7 trillion bucks

A total of 17.5 trillion dollars - just for the current - not those discovering harms or dying from here on out from the increasing severity of harms.

Note that the incidence of deaths, severe and serious harms in the Phase 3 clinical trials UNDERSTATE the harms we have discovered subsequent to roll-out.

It is a shame that no-one in the UK or Australia has been able to test the contents of the Oxford/AstraZeneca vials against clinical trials, post marketing authorization reports, adverse event reporting systems and so on.

Jessica Rose posted this article yesterday that attempted a first correlation study attempt of contamination with VAERS. (Also referenced above).

(100) Unacceptable Jessica | Jessica Rose | Substack

"We have established the beginnings of a dose response curve using DNA (ng/dose) against SAEs/total AEs (shown directly below for Pfizer), "

Onwards!

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