An adverse event is any undesirable experience associated with the use of a medical product in a patient. An adverse event to a medical product should be reported to the FDA.

By reporting potential side effects to our products, the information you provide will help us fulfill our responsibility to report to the FDA and our responsibility to ensure the safety of our products.

If you or the individual you are reporting on behalf is experiencing a medical emergency, contact a medical professional prior to reporting the adverse event.