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The Medical Devices Safety Act Seeks To Make It Easier To Sue Bayer And Other Medical Device Manufacturers

Current laws protect medical device manufacturers to the detriment of patients who are being used as human test animals

Tuesday, September 3, 2019 - Women who are suffering from symptoms such as severe pain and heavy bleeding and have been told that they are crazy by their Essure doctor are encouraged to read the reports of others on social media to reassure themselves that, no, they have not lost their mind. Essure symptoms are all too real when the device breaks free from its intended location attached to the inner walls of the Fallopian Tubes and migrates into the uterus where it can become permanently trapped by painful contractions. If an Essure woman waits until such a situation occurs it may be impossible to retrieve the device without also removing the uterus through a partial hysterectomy, the exact dangerous and hazardous surgical procedure the women was told she could avoid by using Essure. Women can apply to join the Essure Problems Facebook Group or go to Twitter.com and follow along with the group's latest developments. With a current enrollment over 42,000 members, the Essure Problems Facebook Group is a closed group and new members must first be approved. One of the initiatives the group has taken on is their political support of legislation that is currently before Congress, a bill titled The Medical Devices Safety Act. Essure birth control device lawsuits lawyers are experienced litigators in cases of harmful drugs and other products have seen the aftereffects of numerous drug recalls.

Most people are unaware that it may be difficult to receive more than mere reimbursement for one's actual monetary losses such as lost wages and medical expenses from winning a lawsuit against a medical device manufacturer given the way today's laws are written. If the US Food and Drug Administration (FDA) classifies a medical device as Class III, the device's manufacturer has protection against punitive damages. Class III medical devices have the potential to physically harm the patient, or as the FDA puts it, devices that "sustain or support life, are implanted, or present potential unreasonable risk of illness or injury." Ironically, most Class III medical devices such as the Essure Birth Control spring are not tested on humans before they are brought to market. Instead, Class III manufacturers are required to conduct post-market human studies which in reality, make unsuspecting patients human test animals, This was recently pointed out in the Netflix documentary "The Bleeding Edge" pointed out. The MDSA urges lawmakers to take social media and not only FDA reports into account when compiling data for post-market surveys.

According to MedTruth.com The Act requires doctors to immediately report Essure complaints directly to the FDA and to cease denying that Essure complaints are legitimate. "The Medical Device Safety Act, a bipartisan bill introduced in April 2017 by Rep. Brian Fitzpatrick (R-PA) and currently co-sponsored by Rosa DeLauro (D-CT), Jan Schakowsky (D-IL), Peter DeFazio (D-OR), Bobby Rush (D-IL) and Lloyd Doggett (D-TX), would make it much easier for consumers to sue Class III, device manufacturers." The above writers of the bill acknowledge that a faulty medical device such as Essure puts patient's lives at risk and that the current laws that protect only the manufacturers and not the patient must be changed.

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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.