Transvaginal Mesh Help Center

Transvaginal Mesh Help Center The FDA has announced stronger regulations on transvaginal mesh and has reclassified the device as

January 2016: The FDA has announced stronger regulations on transvaginal mesh and has reclassified the device as “high risk.” Manufacturers are now required to submit a premarket approval (PMA) application that supports the safety and effectiveness of surgical mesh for the transvaginal repair of POP.

A sign outside the J&J shareholders meeting read, 'J&J needs to clean up their mesh.'
05/02/2017

A sign outside the J&J shareholders meeting read, 'J&J needs to clean up their mesh.'

Mesh Medical Device News Desk, April 30, 2017 ~ At this years annual J&J shareholders meeting, CEO Gorsky promised the company puts patients first. Protesters outside in the streets shared a different view. But did shareholders even see or did they care? While about 30 protesters lined the streets...

More than 800 women in the UK are suing the National Health Service for defective transvaginal mesh implants.
04/19/2017

More than 800 women in the UK are suing the National Health Service for defective transvaginal mesh implants.

Many women allege they are suffering from physical pain as well as mental health issues as a result of the implants.

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