( May 7, 2025, 2:22 PM EDT) -- SEATTLE — “Perforation and migration to the abdominal cavity is an adverse event that is expressly and repeatedly warned of in the official labeling and patient information materials” of the Mirena intrauterine contraceptive device (IUD), its manufacturer argues in a May 6 motion in Washington federal court to dismiss a woman’s claim that she was injured by the allegedly defective device....