US lawmakers recently introduced legislation in the Senate and House of Representatives mandating that the Food and Drug Administration update how it communicates recalls of medical devices, thus improving the overall recall process.
The Medical Device Recall Improvement Act, introduced last month by Sen. Dick Durbin, D-IL, and Rep
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?