(Matthew Perrone – Associated Press)
U.S. health officials said Monday they plan to overhaul the nation’s decades-old system for approving most medical devices, which has long been criticized by experts for failing to catch problems with risky implants and related products.
The Food and Drug Administration announced plans aimed at making sure new medical devices reflect up-to-date safety and effectiveness features. The system targeted by the actions generally allows manufacturers to launch new products based on similarities to decades-old products, not new clinical testing in patients.
The FDA’s move came one day after the publication of a global investigation into medical device safety by more than 50 media organizations, including The Associated Press. Led by the International Consortium of Investigative Journalists, the group found that more than 1.7 million injuries and nearly 83,000 deaths suspected of being linked to medical devices had been reported to the FDA over a 10-year period. Click here to read more.
- Faulty Medical Devices Prompt FDA Approval-Process Overhaul (Fortune)
- FDA to Overhaul More Than 40-Year-Old Process for Approving Medical Devices That Some Say Puts Consumers at Risk (CNBC)
- Medical Devices Harm Patients Worldwide As Governments Fail On Safety (ICIJ)
- How Global Journalists Investigated Medical Device Safety (Associated Press)