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Bayer May Have Double Crossed Essure Women

Consumer health advocates are growing more and more concerned that Bayer may have pulled a fast one and are really selling more Essure birth control devices than ever

Wednesday, May 1, 2019 - Essure women who were originally elated when Bayer stated they would no longer be selling Essure are now not so sure. Essure doctors, many of who are receiving indirect payments from Bayer are continuing to advise women to have the procedure and are using the Essure devices they have stocked up on or buying those that are readily available on the internet. As a matter of fact, Essure doctors may be recommending Essure more than ever since they may have invested hundreds of thousands of dollars in Essure inventory in 2018 in anticipation of not being able to get them after the first of the year when Bayer stated they were going to stop selling the device. Bayer has been of absolutely no help in dissuading women from using Essure as the company continues to publicly state that they stand behind Essure's risk/reward profile and that there are hundreds of thousands of women that are completely satisfied with Essure performance. Nowhere on the Essure home page are consumers alerted that Essure is no longer for sale and Bayer has stressed that taking Essure off of the market is purely for financial reasons. To this day Essure sales continue unabated at doctor's offices around the United States as well as at Planned Parenthood, the most influential of all birth control organizations, where young women are urged to use the device.

In addition, Essure women are concerned that the post-market studies of Essure that the FDA promised would be forthcoming have been delayed by years allowing millions of more women to potentially fall victim to Essure failed and fraudulent concept. Essure women led by the Founder of the Facebook group Essure Problems, Angie Firmalino, were adamant that the product is taken off of the market at least until a time that more thorough testing could be conducted. Essure birth control device lawsuit attorneys representing women and family members of women harmed by the faulty birth control device and recommend a free consultation before filing a claim.

It appears that things were going consumer advocate's way when in 2016 the FDA required the company to update the warning label on the product as well to require Essure doctors to complete a warning checklist with each new patient and to have the patient sign that they understood Essure's risks. Undercover women posing as potential Essure patients continue to find Essure sales literature in doctor's offices and also were shocked when they conducted exit interviews with Essure patients and most of whom said that they signed no such checklist. In conjunction with the warning label and client checklist, Bayer was required to begin gathering data and conducting an official post-market study however the study has been put off as the results are not required to be submitted until 2023.

Bottom line, Essure is still very much on the market and no post-market study is currently being done. Essure women are not being required to review and sign the patient checklist nor are they exposed to the product's warning label.

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