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The FDA advises patients who have had the Sprint Fidelis lead implanted to contact their doctors, especially if they have experienced the following symptoms:
Additionally, women have experienced side effects including severe pain and cramping, blood clots, infection, pelvic pain, depression, weight gain, and extreme fatigue. From 2002-2013, the FDA received approximately 988 reports citing adverse events related to Essure.
Our team of product liability attorneys are experienced in successfully representing women nationwide in cases involving dangerous pharmaceuticals and defective medical device injuries, including transvaginal mesh, Yaz, and Mirena.