Did you have problems with your Essure implant?
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Bayer, the manufacturer of Essure removed the device from the market in the United States at the end of 2018.
The FDA has received nearly 15,000 adverse event reports related to Essure
The FDA ordered Bayer, the company that makes Essure, to conduct a postmarket surveillance study to gather more data about Essure’s benefits and risks.
The most frequent device problems reported were patient-device incompatibility (2,402) (for example, possible nickel allergy), migration of the device or device component (1,485), device operating differently than expected (663), device breakage (617), device difficult to remove (304), malposition of the device (261), and device difficult to insert (257).
Among the reports are nearly 9,000 surgical removals of Essure, mostly by hysterectomy.
You may be entitled to compensation. Please take this 3 minute evaluation if affected.
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The medical device(s) described on this page remain approved by the United States Food & Drug Administration (FDA).
Please note: completion of this evaluation does not guarantee compensation. Each project has specific qualifying criteria and the criteria may change from time-to-time. In some instances, users who are not immediately contacted may be contacted at a later date.
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