www.fdanews.com/articles/145287-hauser-calls-out-the-fda-guidant-on-recalled-devices
Hauser Calls Out the FDA, Guidant on Recalled Devices
April 2, 2012
It was the death of a 21-year-old patient whose implanted cardiac defibrillator failed to shock his heart back to normal rhythm that started Dr. Robert Hauser on the path to becoming a vocal advocate for change at the FDA.
Mass Device
Mass Device