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Chicago defective medical device lawyersOver the last decade, an estimated 750,000 women have received the Essure birth control implant. Thousands have reported health complications, some of which were life-altering. In response, the U.S. Food and Drug Administration has moved to issue a “black box” warning – their most serious type – for Essure. Yet the devices remain on the market. If you or someone you love has the Essure implant, the following information covers what you should know about the possible risks, and what you can do, should you experience any of them.

Current Warning Label and Potential Complications

Pitched as the only non-surgical permanent birth control option, Essure consists of two nickel-titanium coils. They are implanted into the fallopian tubes, through the cervix, during a 15-minute procedure. Within three months, scar tissue is supposed to develop around the coils, preventing the fallopian tubes from releasing eggs into the uterus. Until a follow-up check at that three-month mark, women are told to use alternative forms of contraception to prevent pregnancy. The device’s current warning says women may experience pelvic pain and bleeding immediately after the procedure.

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