Bayer has said it is progressing with its settlement talks with attorneys for thousands of women who were injured by Essure birth control implants. According to news reports, the company announced that it has set
Women in the United Kingdom have united to stop potentially dangerous vaginal mesh surgical procedures from being offered at clinics and hospitals, according to a news report in Science Times. This is a procedure that
The U.S. Food and Drug Administration (FDA) has issued a Class I recall for the Endologix Ovation iX Abdominal Stent Graft System because of the risk of severe injury or death. According to an FDA
The U.S. Food and Drug Administration (FDA) on April 24th released data from more than 15,000 new adverse event reports in 2019 regarding Essure birth control devices. According to the report, the most common reports
Women in Canada filed a transvaginal mesh class-action lawsuit, which Boston Scientific has agreed to settle for $21.5 million. According to news reports, the proposed settlement involves about 325 women whose share of the settlement
Researchers with the U.S. Food and Drug Administration (FDA) who conducted a long-term study of women implanted with transvaginal mesh to treat pelvic organ prolapse (POP) concluded that the FDA should have banned the products
Mavidon, a medical device manufacturer specializing in products for the application of electrode leads and therapy products, has recalled several of its products for potential bacterial contamination. According to a news release from the US
Attorney General Ellen Rosenblum has filed a lawsuit against Johnson & Johnson for alleged deceptive marketing of its transvaginal mesh devices. According to a news report, the suit also names J&J’s subsidiary Ethicon Inc. Rosenblum
If you received Allergan textured breast implants, you are likely extremely concerned about developing breast-implant-associated anaplastic large cell lymphoma (BIA-ALCL), a cancer of the immune system, which has been linked to textured implants. Last summer,
Johnson & Johnson is issuing a recall for a surgical stapler after reports that seven patients were seriously injured and one died. According to news reports, the medical device, manufactured by Johnson & Johnson’s Ethicon
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