On March 7, 2018, FDA Commissioner Scott Gottlieb released a statement regarding the agency’s ongoing monitoring and investigations into issues related to Bayer‘s controversial birth control device Essure. More than 750,000 women have received the implant since Essure’s approval in 2002. As of December 31, 2017, the FDA has received 26,773 medical device reports related …. Read More
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Nine Scottish women are suing the makers of birth control device Essure after becoming pregnant post-implantation. The device was billed as a simple and safe procedure and an alternative to sterilization, yet many of the women claimed to have experienced excruciating pain, bloating, bleeding and infections. Moreover, the women who became pregnant while implanted with …. Read More
Following thousands of complaints lodged against Bayer, maker of permanent contraceptive device Essure, the company has discontinued sales and marketing of Essure in every country outside the United States. Essure has caused many women to experience unwanted side-effects including migrations, perforation of the uterus or other organs, and chronic pain—many even needing surgery to remove …. Read More
“I went from being a mum who was doing everything with her children, to a mum that was stuck in bed unable to move without pain, at some points being suicidal,” recalls Laura Linkson, mother of three, who suffered severe complications from permanent contraceptive device Essure. Laura was implanted with the device, a small flexible …. Read More
Last Wednesday (8/30/2017), the controversial contraceptive device, Essure, was removed from the Australian market after reports of unintended pregnancies, chronic pain and medical problems continued to surface. A ‘hazard alert’ was issued to inform medical professionals and patients of the device’s dangers by the Department of Health’s Therapeutic Goods Administration (TGA) and by Australasian Medical …. Read More