The Essure birth control device has faced growing scrutiny due to serious and long-term side effect reports.
It was originally marketed as a permanent, non-surgical birth control option for women.
However, rising safety concerns have triggered multiple FDA labeling changes, investigations, and public warnings.
Common Complications Linked to the Essure Birth Control Device
The device, manufactured by Bayer, is a small metal coil inserted into the fallopian tubes. Over time, scar tissue forms around the coils to block the tubes and prevent pregnancy. While this method was promoted as minimally invasive and effective, thousands of women have reported adverse effects following implantation.
The most commonly reported complications from the Essure birth control device include chronic pelvic pain and pain during sexual activity. Other symptoms include persistent headaches, mood disorders such as anxiety or depression, abnormal bleeding, and in some cases, hair loss. Some women also experienced allergic reactions to the materials used in the device, particularly to metals like nickel. In more severe situations, the device shifted from its original position, leading to organ perforation or unintended pregnancy. These complications have sometimes required surgical removal of the device to relieve symptoms or prevent additional harm.
The U.S. Food and Drug Administration (FDA) has received thousands of complaints about the Essure birth control device. It continues to review reports and assess the long-term safety of the product. Although the FDA issued labeling updates, including a black box warning and a patient checklist, serious safety concerns remain. The manufacturer stopped selling the device in the United States in 2018. However, many women who previously received the implant continue to report serious and lasting health issues.
Legal Support for Women Harmed by Essure
If you believe you’ve experienced complications linked to the Essure birth control device, it is critical that you seek medical attention as soon as possible. Your physician can assess your symptoms and determine if the device is contributing to your condition. In some cases, imaging tests or surgical consultation may be necessary to identify and address complications.
At Loncar Lyon Jenkins, we are actively monitoring the situation and reviewing cases involving injuries related to the Essure birth control device. If you or a loved one has suffered from pain, complications, or emotional distress after receiving the Essure implant, you may be eligible for legal action. Our team is available to answer your questions and help you understand your legal options.
Call us today at 800.285.4878 for a free consultation and to learn more about how we can help.