Essure

The FDA has received thousands of reports of serious side effects by users of the Essure permanent birth control device
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Essure

Essure is a permanent, non-surgical birth control device for women first approved for use in the United States in 2002. It is considered less invasive than surgical alternatives because it doesn’t require an incision. However, Bayer, the manufacturer of Essure, has been subject to over 14,000 reports of adverse side effects including organ perforation, autoimmune disorders, subsequent hysterectomies, and device migration.

The FDA recently mandated that the manufacturer update it's product to include a black box warning in order to ensure that patients and providers are fully informed of the risks, side effects, and potential complications of the device prior to making clinical decisions.

In July of 2018, Bayer announced plans to stop selling the Essure device in the United States by the end of the year.

Complications associated with Essure Birth Control include: Abdominal Pain, Pelvic Pain, Organ Perforation, Bleeding, Allergic Reactions, And Other Serious Injuries, many of which often require surgical removal of the device.

If you or a loved one were implanted with an Essure Birth Control and later experienced:

  • Surgical Removal of the Device

You may be entitled to significant compensation from the manufacturer.

There are time deadlines to file a claim so don’t wait – act now.

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Essure

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