The US Food and Drug Administration (FDA) has discouraged the use of laparoscopic power morcellation for the removal of the uterus or uterine fibroids because of the risks associated with uterine sarcomas.
Due to potential product defect issues, the manufacturing company, Johnson & Johnson, agreed to withdraw the medical devices from the market in July 2014.
If you have suffered injuries because of laparoscopic power morcellation, speak to our attorneys.
Our firm is continuing to investigate the use of this device and is offering free initial consultations to victims.
Zoll & Kranz – Defective Medical Drug and Device Lawyers
ZK’s Tidbit: An estimated 8,500 women die each year in the U.S. due to cancer of the uterine corpus.