PROOF!!! Here are recommendations from 2000, 2006, and 2020.
BREAST IMPLANTS are the most controversial and most studied medical device on the market. Now ask yourself WHY the FDA and industry want LESS screening and less information given to patients. Look how watered down and vague the language is in 2020 compared to more detail in the early 2000’s. Less screening means less data, less data is how they keep saying “there’s not enough scientific information to prove lack of safety.”
Why does the FDA and industry want less data instead of more data on a device that is causing cancer and autoimmune illness in patients? What else are they hiding? Remember they were hiding almost SIX MILLION reports of patients harmed by medical devices? #WhatAreYouHiding ~Robyn Towt
