Endo to Stop AMS Mesh Production
Endo International PLC disclosed it is officially closing its women’s health division and stopping the manufacture and sale of transvaginal mesh products. Endo disclosed this after release of...
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FDA labels Transvaginal Mesh High-Risk
The Federal Drug Administration (FDA) has labeled Pelvic Organ Prolapse (POP) devices as “high risk”, after thousands of injuries had been reported. The FDA noted more than...
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Equal Rights Advocates 2015
On June 11, 2015, Rachel Abrams, and others from Levin Simes Abrams attended the 2015 Equal Rights Advocates Gala Luncheon—Forging Ahead—where we celebrated ERA’s 41 years of groundbreaking...
ReadEthicon/Gynecare Recalls Four Transvaginal Mesh Products, Restricts the Usage of Others
After being sued by over 600 women who claim that their transvaginal mesh products caused serious-life altering injuries, Johnson & Johnson’s Ethicon unit has decided to stop selling four...
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