A new Netflix Original documentary titled The Bleeding Edge takes a look at the $400 billion medical device industry in America, and the dangers that come with manufacturing products like hip implants, vaginal mesh, Essure birth control, and robotic surgery devices in a corrupted system. [Read more…]
Fifteen patients at Greenville Medical Center in South Carolina have been diagnosed with a rare infection known as non-tuberculosis mycobacteria (NTM), which has been linked to heater-cooler devices (HCDs) used in certain heart and lung operations. Four out of the fifteen patients have already died from the infections. [Read more…]
The U.S. Food and Drug Administration (FDA) has announced a public hearing forum to take place on November 9-10, 2016 with regard to the enforcement of rules relating to off-label drug and medical product use in the public health industry. The registration deadline to present at the hearing is October 19, 2016, and the deadline for written commentary after the hearing is January 9, 2017. [Read more…]
According to a new study from Northwestern Medicine published in the journal Obstetrics and Gynecology, 22% of a series of high-risk medical devices approved for use in women between 2000 and 2015 won FDA approval based on flawed safety data. [Read more…]
New York, NY, August 24, 2015 — Wendy R. Fleishman of the national plaintiffs’ law firm Lieff Cabraser Heimann & Bernstein, LLP, announces that the firm has published an informational video on IVC blood clot filter injuries and a list of Answers to Frequently Asked Questions About IVC Blood Filters concerning alleged defects in certain retrievable inferior vena cava (IVC) blood filters.