DES MOINES, Iowa — In wake of thousands of consumers reporting major health complications as a result of their Essure implant, the FDA has required that more safety studies will be executed, as reported by KCCI Des Moines.

Marcia Sampson was implanted with Essure five years ago by her doctor after the birth of her fourth child.

Sampson details the implant process as pain free but was later afflicted with excruciating pain that went unidentified as Essure related until she became pregnant, unaware that her birth control device had failed.

The pregnancy ended in a miscarriage which led to Sampson discovering the group ‘Essure problems’ in which she realized that when it came to Essure defects, “it’s not just me.”

Because of reports from the likes of Marcia Sampson, the FDA now requires them to carry a warning label detailing the permanent side effects it can cause.

Sampson worries as she is “finding a lot of ladies don’t sit down and research, I know I didn’t.”

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