If you or a loved one contracted gynecologic cancer after the laparoscopic removal of uterine fibroids, contact the experienced lawyers at Neumann Law Group for a free case evaluation today.

Johnson & Johnson issued a world-wide medical device recall for all power morcellation devices in July of 2014. Later that year, the FDA had manufacturers still producing the devices to include a black box warning label that use of the power morcellator during fibroid surgery may spread cancer and decrease the long-term survival of patients. Nevertheless, other companies continue to make the device, promoting them for continued use.