(June 23, 2012)
Earlier this month, medical device manufacturer Johnson & Johnson (J&J) announced that it would terminate production and sales of four of its Ethicon pelvic mesh implant...
Johnson & Johnson Will Stop Selling Transvaginal Mesh
(June 6, 2012)
Hundreds of thousands of women suffer from a condition called pelvic organ prolapse (POP) and stress urinary incontinence (SUI). POP is diagnosed in patients where the tissue that...
FDA Ordering Risk Study for Implantable Surgical Mesh
January 12, 2012 – In a report from The New York Times, the U.S. Food and Drug Administration (FDA) has ordered the makers of implantable surgical mesh to study the risks of using the product. Implantable surgical...