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The Medical Device Safety Act Seeks To Hold Medical Device Makers Accountable

If a manufacturer is faced with billions of dollars of potential lawsuits they will certainly think twice before rushing a product to market

Monday, April 22, 2019 - Under today's laws, it may be difficult to hold the maker of a faulty Class III medical device accountable for bringing a faulty product to market. FDA, Class III medical devices "... usually sustain or support life, are implanted, or present potential unreasonable risk of illness or injury. Examples of Class III devices include implantable pacemakers and breast implants. 10% of medical devices fall under this category" according to the Food and Drug Administration. The Medical Devices Safety Act of 2017 seeks to change all that. According to MedTruth.com, "Advocates and activists along with 14 individuals harmed by Essure, mesh, breast implants and hip replacements are traveling to Washington to lobby representatives in May (2019), which is when the bill will be reintroduced to the new Congress, Amanda Rusmisell, legislative liaison for the 42,000 member Essure Problems Facebook Group, said." If you're a woman suffering from Essure complications and problems you should consider speaking with Essure birth control lawyers for a free consultation before filing a lawsuit claim.

In the two or so years since I have been following the Facebook group titled Essure Problems, I have seen the number of members go from around 10,000 to now over 40,000 and growing. Essure Problems (EP) group is a closed group so that kind of increase is significant. EP's bottom line is generally, that either you or a family member has to have been harmed by Essure and that you want to help and Essure victim gets help. That makes their membership number all the more important. Essure Problems Facebook group is led by Angie Firmalino, the same woman who was featured in the Netflix documentary "The Bleeding Edge" that exposed not only Essure for the problems it was causing but, moreover, the film exposed the Food and Drug Administration's failure to regulate medical devices. The film highlighted former FDA commissioner-turned-whistleblower David Kessler who explained the ins and outs of the FDA's fast-track approval process and railed as to how the system was allowing faulty medical devices to come to market. The upshot of Ms. Firmalino's work, the Netflix film, and others have been to introduce legislation that will help the thousands of women who have been harmed by Essure and other medical devices file claims in court for compensation for their expenses and pain and suffering in general.

Device migration can cause Essure to become lodged in the uterus where painful contractions attempting to expel the foreign object only sink the sharp metal coil deeper and deeper into the tissues causing severe pain as well as extreme bleeding. Most women opt for a complete hysterectomy rather than endure multiple surgeries while a doctor chases Essure fragments around a woman's reproductive organs. Most Essure symptoms stop when the entire Essure device has been removed. The most recent Bayer annual report admits that close to 30,000 lawsuits have been filed against them seeking compensation for the injuries and trauma caused by the Essure Birth Control device. Holding medical device makers accountable for bringing a faulty product to market may be the only way to keep consumers safe.

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No-Cost, No-Obligation Essure Lawsuit Case Review If You or a Loved One Suffered from Essure Problems

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.