Essure Lawsuit

Lawsuits allege that Essure caused perforation of the fallopian tubes, migration of the device, severe pain, abnormal bleeding, and unwanted pregnancies. Many women reported severe complications requiring emergency surgery.

Plaintiffs claim that Bayer failed to adequately warn about serious risks and that the device was defectively designed.

Essure litigation has resulted in significant settlements from Bayer. Thousands of women have filed lawsuits alleging serious injuries from the device.

The FDA strengthened its warnings after receiving thousands of adverse event reports.

Women who had Essure implanted and subsequently experienced device perforation, migration, severe pain, allergic reactions, or unwanted pregnancy may qualify. Medical records documenting the complication are essential.

You must have had the device implanted and developed serious health complications.

If you or a loved one suffered complications from Essure, contact our firm for a free case review. We have experience representing Essure injury claimants.

Deadlines may apply to filing claims, so prompt action is important.