The Essure Sisters, along with members of the Breast Implant Victim Advocacy Group, returned to Washington D.C. to rally and lobby Congress for the passage of H.R. 2164, The Medical Device Safety Act of 2017.
Much to the dismay of American women, Bayer has decided for 'commercial' reasons to cease selling Essure from the marketplace in every country except the United States. While the women are pleased by the fact that Essure is no longer being sold worldwide, they are angry and frustrated by the lack of action taken in the United States by both ...
Despite a worldwide decrease in demand for Essure, a three month suspension in Europe, a recall in Australia and the device being withdrawn from the market in Finland, the Netherlands, the UK and Canada; its still business as usual in America. FDA and America, wake the hell up.
Calling on all victims of a Class III medical device: A group of medical device advocates, led by the Essure Problems Group, will rally and lobby in Washington D.C. September 25-27th to gain support for the passage of the Medical Device Act of 2017.
As Essure is steadily being banned or discontinued from countries around the world, pressure is mounting for the FDA and Bayer to take decisive action in the United States to remove Essure from the marketplace.
Recently, Brazil has banned the sale of the Essure device and Bayer has announced it is discontinuing distribution in Finland and the Netherlands due to poor sales. Angry victims of Essure want our own FDA to take action and pull this device from the market.