Mask Control: Prove COVID-19 exists...I dare you!

[APAK]

This came out today…..I believe they are recalling the main PCR test (rapid) kits because Gates and Sores are making their own diagnosis testing procedure for OUR future….IMO. And we are to have confidence in these crooks?



Here’s the text of the recall…




BREAKING: FDA Issues Complete Recall For COVID-19 Rapid Tests!

by noah30 mins ago30 mins ago
818views

THIS IS A HUGE BREAKING STORY FOLKS!

I wish I could say I was wrong about this, but sadly I guess I wasn’t.

Remember last year when everyone was rushing out to get “rapid tested” for COVID-19?

The most popular rapid test was the nasal swab, where they basically swabbed the underside of your brain via your nasal cavity and then did it a second time in the other nostril?


Nothing about it ever sat right with me, and whenever I see them pushing something like this on the mass population, my red flags go off.

Turns out, I was right…..those swabs weren’t safe at all or accurate because they have just been recalled by the FDA in a Class I recall.

From FDA.gov itself, take a look:



Yeah, a little late for a recall there FDA, don’t you think?

No one is using them anymore, but good on you for “recalling” them.

Are you also going to recall all the fake data they produced?

All the millions of false positives?

We all knew these things were funky from the beginning!

Remember when Elon Musk did 4 tests at one time and got 2 positive and two negative?

His exact quote: “Something extremely bogus is going on here.”

Follow on Telegram @WeLoveTrumpNoah
Turns on the eccentric billionaire genius rocket scientist was right again, image that.

Here’s more on the story:

“The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.” Innova Medical Group Recalls SARS-CoV-2 Antigen Rapid Qualitative Test

— Katie Pavlich (@KatiePavlich) July 25, 2021



-----------continued ------

 

[APAK]

The FDA announced today that the CDC PCR test for COVID-19 has failed its full review.

Its Emergency Use Authorization has been REVOKED.

It is a Class I recall. The most serious type of recall.
Too many false POSITIVES!Innova Medical Group Recalls SARS-CoV-2 Antigen Rapid Qualitative Test

— 404_Not_Found (@4_04_Not_Found) July 25, 2021



PCR test to be withdrawn – not fit for purpose !

The FDA announced today that the CDC PCR test for COVID-19 has failed its full review.

Its Emergency Use Authorization has been REVOKED.

It is a Class I recall. The most serious type of recall.

Too many false POSITIVES! pic.twitter.com/XN1JTWJpEd

— Fran (@Fran73113786) July 22, 2021



Served its purpose?

Inflated the false positives?

Could it be once again that false positive tests are being used to help the numbers surge?
Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results | FDA Innova Medical Group Recalls SARS-CoV-2 Antigen Rapid Qualitative Test

— Fat Dragon Productions (@fatdragonpro) July 17, 2021



Basically what we are all thinking right now:

Are you freaking kidding me? https://t.co/exEqkFxl4w

— Steve Deace (@SteveDeaceShow) July 25, 2021



Here is the FULL info direct from the FDA.gov website, read it for yourself folks:

Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.


Recalled Product

• Innova SARS-CoV-2 Antigen Rapid Qualitative Test (also distributed under the names Innova COVID-19 Self-Test Kit (3T Configuration), Innova SARS-CoV-2-Antigen Rapid Qualitative Test (7T Configuration), and Innova SARS-CoV-2-Antigen Rapid Qualitative Test (25T Configuration))
• Lot codes:
  • 25T (25 tests per box) – U2101750, U2101751, X2006004, X2008001, X2008010, X2009002, X2009004, X2009013, X2009016, X2010004, X2010010, X2011005, X2011006, X2011007, X2011008, X2011009, X2011012, X2011013, X2011015, X2011016, X2011017, X2011025, X2011051, X2011052, X2012001, X2012002, X2012004, X2012005, X2012008, X2101002, X2101004, X2101014, X2101031, X2101038
  • 3T (3 tests per box) – U2102003, X2012310
  • 7T (7 tests per box) – U2101748, U2102001, U2102002, X2012711, X2103792
• Manufacturing Dates: September 1, 2020 to March 3, 2021
• Distribution Dates: November 2, 2020 to March 22, 2021
• Devices Recalled in the U.S.: At least 77,339
• Date Initiated by Firm: March 24, 2021

Device Description
The Innova SARS-CoV-2 Antigen Rapid Qualitative Test claimed to determine if a person has an active COVID-19 infection. The test used a nasal swab sample and test strip to detect specific proteins, called antigens, from the SARS-CoV-2 virus. If the nasal sample had SARS-CoV-2 antigens, a colored test line should have appeared on the test strip, indicating that the person may have COVID-19. If the nasal sample did not have SARS-CoV-2 antigens, a colored line should not have appeared on the test strip. The test has not been authorized, cleared, or approved by FDA for commercial distribution in the United States.

Reason for Recall

Innova Medical Group is recalling its SARS-CoV-2 Antigen Rapid Qualitative Test. Labeling distributed with certain configurations of the test includes performance claims that did not accurately reflect the performance estimates observed during the clinical studies of the tests. The performance characteristics of the test have not been adequately established, presenting a risk of false results.

• False-negative results may lead to delayed diagnosis or inappropriate treatment of SARS-CoV-2, which may cause patient harm including serious illness and death. False-negative results can also lead to further spread of the SARS-CoV-2 virus, including when presumed negative patients are grouped into cohorts in health care, long-term care, and other facilities based on false test results.
• False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results.

Who May Be Affected

• People who were tested using these devices
• Health care providers who may have access to and use these tests or whose patients have used these tests
• Organizers of large testing programs, such as on college campuses, who may be using and distributing these tests for diagnostic use

What to Do
On April 23, 2021, Innova Medical Group sent all affected device users an Urgent Medical Device Recall letter. The letter provided the following information:

• Do not use these tests to screen for or diagnose COVID-19.
• Identify and remove all affected tests from inventory.
• Either destroy the tests by placing them in the trash or return the tests using the FedEx return label that was included with the letter Innova sent to its customers.
• Complete and return the form Innova sent to its customers, indicating the number of destroyed or returned tests.

The FDA also recommends:

• Test users and caregivers: Talk to your health care provider if you think you were tested with the Innova SARS-CoV-2 Antigen Rapid Qualitative Test and you have concerns about your test results.
• Health care providers: If the test was given less than two weeks ago, consider retesting your patients using a different SARS-CoV-2 diagnostic test if you suspect an inaccurate result. If testing was performed more than two weeks ago and there is no reason to suspect current SARS-CoV-2 infection, it is not necessary to retest.
• Testing program organizers: Notify participants in your testing program to discontinue diagnostic use of these tests and to use an FDA-authorized test to continue testing. For listings of FDA-authorized tests, see:
  • FDA-Authorized Molecular Diagnostic Tests for SARS-CoV-2
  • FDA-Authorized Antigen Diagnostic Tests for SARS-CoV-2
• Report any problems you experience with the Innova SARS-CoV-2 Antigen Rapid Test to the FDA, including suspected false results.

For more information, please see the FDA’s June 2021 safety communication, Stop Using Innova SARS-CoV-2 Antigen Rapid Qualitative Test.

Contact Information
Customers with questions about this recall should contact Linda Weinreb at [email protected] or call 747-494-0852.

 

[Enoch111]

False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results.

Everyone should note the lies and baloney in this paragraph even within the recall information posted by FDA:

1. "False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness". A false positive is FALSE POSITIVE. Which means that a healthy individual has been unfairly and unethically labeled as a "case". This person has no illness and needs no treatment. So this is another attempt to obfuscate the truth.

2. "...which could be another life-threatening disease that is not SARS-CoV-2..." The only life threatening diseases are arising from the bogus vaccines. But this has not been clearly stated. In fact completely avoided. More misdirection and fear-mongering by these liars.

3. "False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results." This is total and absolute baloney. It is now well-established that healthy, asymptomatic people who falsely test positive through the PCR test do not infect anyone. They are not carrying the virus, since the CT value is totally misleading, and the test is a FALSE POSITIVE.

As we can see these people simply do not want to tell the public the truth, even after they have been caught out. Neither does FDA or any other government agency.

 

[Cristo Rei]

Thing is though covid isn't the only issue. There is an over powering agenda and Covid is merely one means to the end. Anarchy, taking place world wide, in the guise of protesting, encompasses looting, destruction, and arson. Quiet revolt, or slow riots are now referred to in America as looters and thieves casually wander into stores, fill their bags and wander out again without fear arrest or bring impeded by security.
In south Africa at the moment open looting is under way. And it's organized. Thousands of vehicles cram the motorways adjacent to warehouses, where they are left unattended while the occupants proceed to the warehouse, help themselves to whatever they want, return to their vehicles unmolested. Thousands. It's open anarchy and the police are unable to effectively stop it. But it's organized. And was planned some time ago. View attachment 16332 View attachment 16333 View attachment 16334 View attachment 16335 View attachment 16336

True even Klaus Schwab is warning of a Cyber attack... That's potential power grid off. That's potential frozen bank accounts and even lost money

 

[Cristo Rei]

The FDA announced today that the CDC PCR test for COVID-19 has failed its full review.

Its Emergency Use Authorization has been REVOKED.

It is a Class I recall. The most serious type of recall.
Too many false POSITIVES!Innova Medical Group Recalls SARS-CoV-2 Antigen Rapid Qualitative Test

— 404_Not_Found (@4_04_Not_Found) July 25, 2021



PCR test to be withdrawn – not fit for purpose !

The FDA announced today that the CDC PCR test for COVID-19 has failed its full review.

Its Emergency Use Authorization has been REVOKED.

It is a Class I recall. The most serious type of recall.

Too many false POSITIVES! pic.twitter.com/XN1JTWJpEd

— Fran (@Fran73113786) July 22, 2021



Served its purpose?

Inflated the false positives?

Could it be once again that false positive tests are being used to help the numbers surge?
Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results | FDA Innova Medical Group Recalls SARS-CoV-2 Antigen Rapid Qualitative Test

— Fat Dragon Productions (@fatdragonpro) July 17, 2021



Basically what we are all thinking right now:

Are you freaking kidding me? https://t.co/exEqkFxl4w

— Steve Deace (@SteveDeaceShow) July 25, 2021



Here is the FULL info direct from the FDA.gov website, read it for yourself folks:

Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.


Recalled Product

• Innova SARS-CoV-2 Antigen Rapid Qualitative Test (also distributed under the names Innova COVID-19 Self-Test Kit (3T Configuration), Innova SARS-CoV-2-Antigen Rapid Qualitative Test (7T Configuration), and Innova SARS-CoV-2-Antigen Rapid Qualitative Test (25T Configuration))
• Lot codes:
  • 25T (25 tests per box) – U2101750, U2101751, X2006004, X2008001, X2008010, X2009002, X2009004, X2009013, X2009016, X2010004, X2010010, X2011005, X2011006, X2011007, X2011008, X2011009, X2011012, X2011013, X2011015, X2011016, X2011017, X2011025, X2011051, X2011052, X2012001, X2012002, X2012004, X2012005, X2012008, X2101002, X2101004, X2101014, X2101031, X2101038
  • 3T (3 tests per box) – U2102003, X2012310
  • 7T (7 tests per box) – U2101748, U2102001, U2102002, X2012711, X2103792
• Manufacturing Dates: September 1, 2020 to March 3, 2021
• Distribution Dates: November 2, 2020 to March 22, 2021
• Devices Recalled in the U.S.: At least 77,339
• Date Initiated by Firm: March 24, 2021

Device Description
The Innova SARS-CoV-2 Antigen Rapid Qualitative Test claimed to determine if a person has an active COVID-19 infection. The test used a nasal swab sample and test strip to detect specific proteins, called antigens, from the SARS-CoV-2 virus. If the nasal sample had SARS-CoV-2 antigens, a colored test line should have appeared on the test strip, indicating that the person may have COVID-19. If the nasal sample did not have SARS-CoV-2 antigens, a colored line should not have appeared on the test strip. The test has not been authorized, cleared, or approved by FDA for commercial distribution in the United States.

Reason for Recall

Innova Medical Group is recalling its SARS-CoV-2 Antigen Rapid Qualitative Test. Labeling distributed with certain configurations of the test includes performance claims that did not accurately reflect the performance estimates observed during the clinical studies of the tests. The performance characteristics of the test have not been adequately established, presenting a risk of false results.

• False-negative results may lead to delayed diagnosis or inappropriate treatment of SARS-CoV-2, which may cause patient harm including serious illness and death. False-negative results can also lead to further spread of the SARS-CoV-2 virus, including when presumed negative patients are grouped into cohorts in health care, long-term care, and other facilities based on false test results.
• False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results.

Who May Be Affected

• People who were tested using these devices
• Health care providers who may have access to and use these tests or whose patients have used these tests
• Organizers of large testing programs, such as on college campuses, who may be using and distributing these tests for diagnostic use

What to Do
On April 23, 2021, Innova Medical Group sent all affected device users an Urgent Medical Device Recall letter. The letter provided the following information:

• Do not use these tests to screen for or diagnose COVID-19.
• Identify and remove all affected tests from inventory.
• Either destroy the tests by placing them in the trash or return the tests using the FedEx return label that was included with the letter Innova sent to its customers.
• Complete and return the form Innova sent to its customers, indicating the number of destroyed or returned tests.

The FDA also recommends:

• Test users and caregivers: Talk to your health care provider if you think you were tested with the Innova SARS-CoV-2 Antigen Rapid Qualitative Test and you have concerns about your test results.
• Health care providers: If the test was given less than two weeks ago, consider retesting your patients using a different SARS-CoV-2 diagnostic test if you suspect an inaccurate result. If testing was performed more than two weeks ago and there is no reason to suspect current SARS-CoV-2 infection, it is not necessary to retest.
• Testing program organizers: Notify participants in your testing program to discontinue diagnostic use of these tests and to use an FDA-authorized test to continue testing. For listings of FDA-authorized tests, see:
  • FDA-Authorized Molecular Diagnostic Tests for SARS-CoV-2
  • FDA-Authorized Antigen Diagnostic Tests for SARS-CoV-2
• Report any problems you experience with the Innova SARS-CoV-2 Antigen Rapid Test to the FDA, including suspected false results.

For more information, please see the FDA’s June 2021 safety communication, Stop Using Innova SARS-CoV-2 Antigen Rapid Qualitative Test.

Contact Information
Customers with questions about this recall should contact Linda Weinreb at [email protected] or call 747-494-0852.

Even the WHO said that the tests are no good.
They also said that lockdowns are no good.
Yet the government's keep using them

We'll keep an eye on these developments...
I'm guessing government's will ignore this and keep using the test... Ours will for sure

 

[Brakelite]

True even Klaus Schwab is warning of a Cyber attack... That's potential power grid off. That's potential frozen bank accounts and even lost money

He's a Freemason, and it's likely they who are controlling those very cyber attacks in order to escalate the rioting.

 

[Cristo Rei]

@APAK @Enoch111 @Backlit

Talk to me about the Fauci trial...

What kind of court is it?
What is he being charged for?

I recently saw Rand Paul (seemingly the prosecuting attorney) set up Fauci to expose the fact that he lied in court.
He said that he was never involved in a "gain of function" research when there is proof now that he was.

This should change everything...
Lying to a court is purgery, punishable by up to 10 years prison over here.

Fauci should be immediately incarcerated but instead he is still the chief health officer for the USA...
This is unreal. He should at least get stood down while the case is being heard.

Do u guys think that justice will be served in this hearing or are the courts corrupted as well?

 

[Enoch111]

Fauci to expose the fact that he lied in court.

Fauci has lied to Congress and the Senate about his involvement with the Wuhan Virus. And he has lied about everything else regarding COVID also. So Senator Rand Paul (who was a medical doctor) has sent a request to the Department of Justice (DOJ) to open a criminal investigation into Anthony Fauci. If you have not read the Fauci Dossier you should do so. Type in The Fauci COVID-19 Dossier into your search engine. It is in PDF format.

Chances are that the DOJ will do absolutely nothing. Which means that Paul will have to do something about that. The DOJ and FBI have now become the arch criminals in the USA.

 

[Cristo Rei]

Fauci has lied to Congress and the Senate about his involvement with the Wuhan Virus. And he has lied about everything else regarding COVID also. So Senator Rand Paul (who was a medical doctor) has sent a request to the Department of Justice (DOJ) to open a criminal investigation into Anthony Fauci. If you have not read the Fauci Dossier you should do so. Type in The Fauci COVID-19 Dossier into your search engine. It is in PDF format.

Chances are that the DOJ will do absolutely nothing. Which means that Paul will have to do something about that. The DOJ and FBI have now become the arch criminals in the USA.

Ok...
Is this the same DOJ that saw Biden steal the election? No justice will come of this I think.
The DOJ is corrupt as well. They wouldn't have executed the plan without buying the DOJ as well...

Will there ever be justice for these demons in this world... Maybe not, but unless they truly repent with tears of blood they will burn in hell

 

[APAK]

Everyone should note the lies and baloney in this paragraph even within the recall information posted by FDA:

1. "False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness". A false positive is FALSE POSITIVE. Which means that a healthy individual has been unfairly and unethically labeled as a "case". This person has no illness and needs no treatment. So this is another attempt to obfuscate the truth.

2. "...which could be another life-threatening disease that is not SARS-CoV-2..." The only life threatening diseases are arising from the bogus vaccines. But this has not been clearly stated. In fact completely avoided. More misdirection and fear-mongering by these liars.

3. "False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results." This is total and absolute baloney. It is now well-established that healthy, asymptomatic people who falsely test positive through the PCR test do not infect anyone. They are not carrying the virus, since the CT value is totally misleading, and the test is a FALSE POSITIVE.

As we can see these people simply do not want to tell the public the truth, even after they have been caught out. Neither does FDA or any other government agency.

I'm waiting for the other shoe to drop when they try to explain away the causes of vaxx deaths as the deaths keep mounting up. They will make some convincing explanation for the sheeple and will say we have a new and safer poison for your body, and they will get FDA approval for these newer so-called vaccines...in 3-6 months time

 

[Cristo Rei]

I'm waiting for the other shoe to drop when they try to explain away the causes of vaxx deaths as the deaths keep mounting up. They will make some convincing explanation for the sheeple and will say we have a new and safer poison for your body, and they will get FDA approval for these newer so-called vaccines...in 3-6 months time

Ye novavax... Have u heard of it? Their saying its 100% safe and effective... It works differently to mrna.
It uses spike proteins from moths... I'll try track down the interview i saw this in recently... Stay tuned. Its a new one

 

[Cristo Rei]

But first... its meme time...



Logic 101

 

[APAK]

Ye novavax... Have u heard of it? Their saying its 100% safe and effective... It works differently to mrna.
It uses spike proteins from moths... I'll try track down the interview i saw this in recently... Stay tuned. Its a new one

No I have not heard of it yet...I'm not surprised at all Cristo..they have to fix their marketing scheme with something else and new....to keep 'us' all off guard during these evil times indeed.

 

[Cristo Rei]

No I have not heard of it yet...I'm not surprised at all Cristo..they have to fix their marketing scheme with something else and new....to keep 'us' all off guard during these evil times indeed.

Its already happening bro...

The interview is almost 30mins long. They talk about a few things and its very interesting...
The part where she talks about this Novavax needle start at 16:30... Please listen to it and tell me your thoughts

https://banned.video/watch?id=60fb3ec7a43f7c0b59f57b9d

 

[APAK]

Its already happening bro...

The interview is almost 30mins long. They talk about a few things and its very interesting...
The part where she talks about this Novavax needle start at 16:30... Please listen to it and tell me your thoughts

https://banned.video/watch?id=60fb3ec7a43f7c0b59f57b9d

Vey informative, This NOVAVAX from Gaithersburg VA I believe is more deadly that the current poisons they are peddling. I agree with this doctor. This one specializes in giving you 'mad cow' disease beside the usual 'heartfelt' blood clots

 

[Cristo Rei]

Vey informative, This NOVAVAX from Gaithersburg VA I believe is more deadly that the current poisons they are peddling. I agree with this doctor. This one specializes in giving you 'mad cow' disease beside the usual 'heartfelt' blood clots

I said yuk when i heard that... Spider virus... moths... No way
Choose your poison... DNA modification or a spider virus grown in moths

 

[Enoch111]

I'm waiting for the other shoe to drop when they try to explain away the causes of vaxx deaths as the deaths keep mounting up.

They all are now blaming the unvaccinated for the vaccine deaths! That is how wicked this whole conspiracy has become. They want to force the unvaccinated to be infected, and they want the vaccinated to wear masks. At the same time the FDA has finally realized that the PCR tests are simply baloney. The media has been fear-mongering with a "Casedemic" when probably 99% of those cases were false positives. The range of false positives has been given as 70-90% but I believe that is simply to avoid total embarrassment.

 

[Brakelite]

So I just received a short video and a random dude going to the VAERS website. He showed precisely how he entered the query to find out how many deaths. What he did looked perfectly legit. The answer came up...
There are 51,347 rows (deaths), but can only show details for no more than 10,000.

 

[Josho]

Vaccine sceptic and Hillsong Church member dies from covid

 

[Cristo Rei]

Vaccine sceptic and Hillsong Church member dies from covid

Who cares

In Australia there have been over 40,000 reports of adverse events including 400 deaths after taking the experimental needle

Right now there are 25 people in hospital and 6 in ICU with TTS from the experimental syringe...
Its doing more damage than covid in Australia and there has only been 10 million doses administered...