Recent publications by whistleblower Melissa McAtee reveal a disturbing picture. When Pfizer's COVID-19 mRNA product became mandatory for personnel at a manufacturing plant in the United States in August 2021, employees of the pharma giant founded a chat group called "Phyzer Vaxx Council".
Hundreds of employees joined the group, including high-ranking individuals in management positions. Every day they "discussed the evils that were done", and the things they were supposed to "just pretend was normal".
In the group chat, it appears that employees expressed concerns about the number of batches with issues, and the covering up of expired product with new labels.
Notably, one such message conveys serious negligent behavior that shows a reckless disregard for the safety and well-being of others:
"Not to mention the cold storage times. And having to change times to just to make it work. Or peeling expired product to relabel it with new dates."
The screenshots were shared on 30 Dec 2023, along with internal emails, and proof of employment, and have previously never been seen or posted anywhere else. Names have been blackened to protect those who are still employed, or who have not consented to the publication of their names.
McAtee mentioned that the documents were being published late due to heavy censorship, and expressed concerns about her safety after releasing the documents to the public with the promise of more to follow in 2024.
I am NOT suicidal. I am NOT depressed. My car is in full functioning capability. I’ve had no gas work done at my home. I love my life and family.
In another tweet she points out that people are misinterpreting her statements and making the wrong assumptions about her views, emphasizing that her position at the Pfizer plant was that of a pharmaceutical quality auditor. As a quality auditor her job was to raise quality concerns.
In the documents there may be several abbreviations that require further explanation. These include:
🔹 QAR: Quality Assurance Review - An assessment of the quality of a product or process to ensure it meets certain standards.
🔹 MIR: Manufacturing Investigation Report - A document that details the findings of an investigation into a manufacturing issue.
🔹 ER: Exemption Report - An Exemption Report (ER) is a document that explains why a product or process is exempt from certain regulations or standards.
🔹 CPM: Carpujects Fill Line - A specific type of equipment used to fill syringes.
🔹 M19: Another fill line that fills Carpujects
The documents have raised serious concerns about the integrity and safety of the COVID-19 mRNA-product's manufacturing process at Pfizer's U.S.-based plant, highlighting potential issues that could have impacted the quality and safety of the product.
Failure to adhere to pharmaceutical safety protocols is a serious form of gross negligence. However, it should be noted that the claims have not yet been independently verified, and further investigation is needed to determine their authenticity and accuracy.
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