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Mirena IUD Lawsuits Move Forward, With Issuance of New Case Management Orders in New Jersey Litigation, Bernstein Liebhard LLP Reports
Date:9/28/2013

na IUD Products Liability Litigation, MDL No. 2434) All of the claims accuse Bayer Healthcare Pharmaceuticals of failing to provide adequate warnings regarding the possibility of spontaneous migration and related complications, and of exaggerating Mirena’s benefits while downplaying its risks. Some of the Mirena complications allegedly suffered by these plaintiffs include uterine perforations, uterine embedment, ectopic pregnancy, infections, and scarring.

Recent media reports indicate that the U.S. Food & Drug Administration (FDA) has received more than 70,000 complaints involving Mirena complications, including instances of device dislocation and uterine perforation, since the IUD was first approved by the agency as a long-action method of birth control in 2000.* In 2009, Bayer received an FDA Warning Letter which criticized the company for making claims in certain Mirena marketing materials that the agency deemed to be misleading, including some that overstated the IUD’s benefits and downplayed serious Mirena complications.

Victims of alleged Mirena complications may be entitled to compensation for medical expenses, lost wages, pain and suffering, and more. Learn More about Mirena IUD lawsuits by visiting Bernstein Liebhard LLP’s website. For additional information, please call 800-511-5092.

*wxyz.com/dpp/news/local_news/investigations/thousands-of-women-complain-about-dangerous-complications-from-mirena-iud-birth-control, 7 Action News, August 27, 2013

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