Essure to be Removed From the Market in The United States

Essure birth control device will be removed from the market, completing a global withdrawal effective by the end of the year

Sunday, July 22, 2018 - Concerned Essure patient and members of the Essure Problems Facebook group, celebrity consumer advocate Erin Brockovich, and several US congressmen have lobbied for years to have Essure pulled from the US market until further testing can be done and now their efforts are being rewarded. The Essure birth control device is going to be taken off of the market globally by the end of 2018 according to an article today in the New York Times.

The Essure birth control device is a small metal coil resembling the spring from a ball-point pen that is implanted in the comfort and convenience of a doctor's office without the need for a hospital stay or general anesthesia. Essure is inserted through the vagina and into both Fallopian tubes where polypropylene fibers create inflammation. Over the next three months, scar tissue builds up and creates a barrier preventing fertilization.

Thousands of women have filed complaints with the US Food and Drug Administration and tens of thousands more have posted stories of their life-altering adverse side effects from using Essure. Essure women suffer severe, permanent and debilitating injuries such as the device migrating away from its intended location on the inner walls of the Fallopian tubes and perforating the uterus. Thousands of women suffer from allergic reactions and auto-immune disorders from the Nickel component of Essure. Bayer maker of Essure continues to claim that Essure is safe and that the market withdrawal is based on economic issues and not a result of consumer complaints. Years ago, Bayer discontinued selling Essure globally with the exception of the US, again for economic reasons, an equally perplexing business decision given the fact that Essure is the world's best-selling birth control device. Women suffering from Essure complications are advised to seek legal counsel in the form of an experienced Essure problems attorney to see if they qualify to file a claim against its maker, Bayer Pharmaceuticals.

Women attempting to have Essure removed have been met with frustration and failure. Essure removal is complex and difficult and very few doctors in the US are willing to attempt to the procedure. Essure often breaks into pieces and fragment can be left behind leaving the patient with the same symptoms that they sought to alleviate with surgery. Essure can become so embedded in scar tissue that a partial hysterectomy is usually required. Other times, perforations of other parts of a woman's reproductive system require a radical hysterectomy to completely remove the device.

Prior to Essure's market withdrawal, in April of 2018, the FDA began requiring Essure doctors to sit down with prospective Essure patients and fill out a questionnaire designed to ensure that the patient had been made aware of Essure's risks. Essure patient has complained of being in constant pain, total body rashes, migraine headaches, and abnormal menstrual bleeding as well as hair and tooth loss. According to reports on social media few doctors complied with the FDA mandate to warn their patients.

Source: https://www.nytimes.com/2018/07/20/health/bayer-essure-birth-control.html

More Recent Essure Complications Lawsuit News:

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• Women from England Report Essure Disasters | 8/15/2019
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• The Medical Devices Guardians Acts Will Force Doctors to Report Essure Patient Complaints | 7/26/2019
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• Essure Causes Ectopic Pregnancies | 7/15/2019
• Essure Women May Elect Preventative Surgery To Remove It Before Extensive Organ Damage Occurs | 7/9/2019
• Essure Removal Doctors Finds The Device Calcifies Causing Excruciating Pain and Potential Organ Perforation | 7/3/2019
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• The Medical Device Safety Act Seeks To Hold Medical Device Makers Accountable | 4/22/2019
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