FDA Bans Transvaginal Pelvic Organ Prolapse Mesh (Apr 2019)
By MeshNewsDesk|2019-04-27T09:47:35+00:00April 27th, 2019|management of mesh complications, Mesh Ban, mesh complications, pelvic floor dysfunction, pelvic floor health, pelvic floor muscles, pelvic mesh removal, Pelvic Organ Prolapse Mesh, pelvic organ prolapse mesh removal, TVT mesh removal|0 Comments
About the Author: MeshNewsDesk
I’m National News Editor, Jane Akre and I began Mesh Medical Device News Desk aka Mesh News Desk (MND) in the summer of 2011 just after the Food and Drug Administration issued an explicit warning to the public that complications associated with surgical mesh used for prolapse repair (POP) and incontinence (SUI) are NOT rare! That was the starting point for the litigation you see today and thousands of lawsuits have been filed by women whose lives have been altered, some permanently, by the use of this petroleum-based product. Patients receiving the same product for hernia repairs are increasingly reporting the same complications. That’s where Mesh News Desk comes in.
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