Medscape

FDA: Continuing Safety Concerns With Transvaginal Mesh

July 13, 2011 — A dramatic increase in reports of adverse events over the use of surgical mesh for the transvaginal repair of pelvic organ prolapse (POP) is a continuing serious safety concern, the US ...
Business Wire

Surgical Mesh - Medical Devices Pipeline Assessment, 2019 - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Surgical Mesh - Medical Devices Pipeline Assessment, 2019" report has been added to ResearchAndMarkets.com's offering. Surgical Mesh - Medical Devices Pipeline Assessment ...
WBUR

FDA Reclassifies Vaginal Mesh, Device Used For Prolapse, As 'High Risk'

The U.S.Food and Drug Administration has moved to strengthen regulations on vaginal mesh, a controversial medical device used to treat pelvic organ prolapse, a condition that can occur after ...
RAPS

FDA highlights updated labeling for some surgical mesh products, cautions against use of mesh in breast surgery

The US Food and Drug Administration (FDA) issued a letter to healthcare providers to make sure they are aware of updated warnings and precautions for certain surgical mesh products produced by Becton, ...