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Bayer Says Essure is Safe and Taking it Off The Market is Purely Business Decision

It is 2019 and Essure is no longer being sold by Bayer

Wednesday, January 9, 2019 - Now that we are a week or so into the new year Bayer has discontinued selling Essure in the US due to business reasons. Bayer has announced to the medical community that their decision to stop selling Essure was "based on a decline in US sales," according to Essure.com, and that being in the Essure business was no longer sustainable. Essure wants its hundreds of thousands of satisfied customers to know that the benefit to risk profile of Essure has not changed and the company stands behind the safety and efficacy of the device. Bayer comes to that safety conclusion after having studied more than 200,000 women that use the Essure birth control device over a period of the last 20 years. Bayer claims to have worked with independent medical researchers that have created an extensive body of knowledge about the device. Essure birth control lawyers represent people and families harmed by the use of Essure birth control device.

Bayer continues to deny that Essure is dangerous to a woman's health as tens of thousands of Essure women have claimed and also that the information being produced in movies, social media, and government agencies such as the FDA is both "inaccurate and misleading." The Netflix documentary movie "The Bleeding Edge" focuses attention on women who have had Essure implanted like Angie Firmalino who claimed to be in extreme and debilitating pain from fever, achy joints, and constant bleeding for months from what was later determined to be an Essure-perforated uterus, after the device broke free from her Fallopian tube and migrated. Firmalino's attempts to have the device completely removed failed and metal fragments were left behind in various locations in her reproductive system. Bayer's claims that the device is safe for woman is contradicted on the very top of the product's home page where the following warning is given: "Some patients implanted with the Essure System for Permanent Birth Control have experienced and/or reported adverse events, including perforation of the uterus and/or fallopian tubes, identification of inserts in the abdominal or pelvic cavity, persistent pain, and suspected allergic or hypersensitivity reactions."

Bayer also claims that the FDA is on their side and that the agency "has for years maintained for several years that the benefits of Essure outweigh its risks," according to the Essure product withdrawal announcement. Such an opinion seems to be at odds with the recent FDA action to place restrictions on the sale of Essure that were so severe as to cause US Essure sales to plummet by around 70% prompting Essure to discontinue offering the product. Essure doctors were and currently are required to have prospective Essure patients read and sign a written checklist of Essure complication to make sure that they are under no delusions as to the risks they are about to undertake. Once a woman is informed as to what has happened to others and could happen to them they seldom think that Essure so-called "risk to reward" profile is worth it.

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OnderLaw, LLC is a St. Louis personal injury law firm handling serious injury and death claims across the country. Its mission is the pursuit of justice, no matter how complex the case or strenuous the effort. OnderLaw has represented clients throughout the United States in pharmaceutical and medical device litigation such as Pradaxa, Lexapro and Yasmin/Yaz, where the firm's attorneys held significant leadership roles in the litigation, as well as Actos, DePuy, Risperdal and others, and other law firms throughout the nation often seek its experience and expertise on complex litigation.