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.

05/04/2017
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.

Transvaginal mesh implants have been linked to dangerous complications
04/17/2017

Transvaginal mesh implants have been linked to dangerous complications

You may be able to seek compensation if you were implanted with transvaginal mesh for pelvic organ prolapse (POP) or stress urinary incontinence (SUI) and experienced side effects like revision surgery, bladder performation, or infection.

The trial against Johnson & Johnson's transvaginal mesh began yesterday. Learn more about it here:
04/11/2017

The trial against Johnson & Johnson's transvaginal mesh began yesterday. Learn more about it here:

Mesh Medical Device News Desk, April 10, 2017 ~ It’s been 14 months since the last product liability trial naming a mesh manufacturer. In this case, Ms. M. Engleman was implanted with two pelvic meshes made by Ethicon, the division of Johnson & Johnson. Jury selection begins today. An army of eight...

After being implanted with Jonson & Johnson's transvaginal mesh without her consent, Lynda Garlinge said, "I felt like I...
03/17/2017

After being implanted with Jonson & Johnson's transvaginal mesh without her consent, Lynda Garlinge said, "I felt like I'd been r***d." Now, she and 450 women are filing lawsuits against J&J.

Lynda Garlinge was implanted with transvaginal mesh, but she didn't know for nearly a decade.

Advocates are lobbying in Australia to take Transvaginal Mesh devices off the market:
03/15/2017

Advocates are lobbying in Australia to take Transvaginal Mesh devices off the market:

A Senate inquiry on pelvic mesh needs to ask the hard questions of our health administrators.

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