The Mirena IUD is a t-shaped intrauterine device which, when implanted in the patient’s uterus by a clinician, claims to prevent pregnancy for up to five years. The Mirena IUD contains a very small (when compared to a common birth control pill) dosage of Levonorgestrel hormone, which is released gradually over time, thus ostensibly preventing pregnancy should the device remain in place. Around two million Mirena IUDs have been implanted in the United States alone.
Were you injured by a Mirena IUD? Contact our Corpus Christi defective medical device lawyers for a free consultation regarding your rights; call (361) 238-2789 today.
Bayer, the maker of the Mirena intrauterine device, has faced numerous claims from consumers regarding the failure of the device, as well as relating to fraudulent marketing practices to both consumers and medical professionals.
A handful of pre-existing claims found in Mirena lawsuits include:
In the case of Mirena lawsuits, the company has been under scrutiny by the FDA since at least 2009 for marketing and advertising claims, which violated the Food, Drug, and Cosmetic Act.
In the incident from 2009, the company was found in breach of the Act by way of making false claims that its IUD device:
Ultimately, the FDA held that the company acted irresponsibly in its advertising and marketing towards a consumer population of generally young women while attempting to avoid known and otherwise documented side effects of the drug such as increased weight, the appearance of acne, and breast pain in the patients. Specifically, the company employed an innovative marketing strategy using third-party marketers to reach out to young women, who otherwise would have been inclined to take the more common oral contraceptive birth control pills. Part of this marketing process entailed downplaying the known risks of IUD implantation, as well as grossly overstating the potential benefits of the IUD.
To date, over 60,000 instances of violations of FDA rules and regulations, as well as adverse medical complications due to the spontaneous migration of the IUD device into the patient’s body cavities, have been substantiated by the FDA since the drug went to market in 2000. To date, the company has still yet to recall the device.
Following growing numbers of lawsuits filed against Bayer across the United States, multi-district consolidations have been initiated, with federal-level multi-district litigation cases consolidating as recently as October of 2015 with numerous class-action suits pending in state jurisdictions. In response, the company has settled some claims individually; however, all class-action litigation cases are pending or accepting new plaintiffs at this time.
If you or someone you care about has been injured or suffered harm as a result of the Mirena IUD, contact Bandas Law Firm, P.C. and discuss your legal options with an experienced Corpus Christi Mirena lawsuit attorney at our firm.
Call (361) 238-2789 or fill out and submit an online contact form to get started with your no-cost consultation.
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