An adverse event is any undesirable experience associated with the use of a medical product in a patient. The event is serious and should be reported to the FDA when the patient outcome is:
- Life-Threatening Injury
- Permanent or Temporary Damage
- Birth Defect
- Other Injuries
If you or a loved one suffered tubal/uterus puncturing, bleeding, or other injuries from Essure, please call our experienced products liability attorneys at (888) 606-5297 for a free consultation about your Essure lawsuit.