More than 1.2 million medical device side-effect reports not submitted within legal timeframe, analysis finds

More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data published by The BMJ.
đ Full Story

Andrew Tate DESTROYS DeSantis For STUPID Comments On Tate Brothers Coming to Florida
- Apple M4 MacBook Air review: I have no notes - Andrew Cunningham
- Brewing Tea Can Remove Toxic Metals From Water, Study Suggests - Simon Spichak
- R-Rated Cop Thriller On Max Unlike Any Movie In The Genre - Robert Scucci
- Garantex administrator arrested in India at request of US authorities - Jagmeet Singh, Lorenzo Franceschi-Bicchierai
- Tense Sci-Fi Crime Thriller On Hulu Lays Low In the Most Unexpected Places - Robert Scucci
- EXCLUSIVE | From Indie Roots to the Oscars: Adam J. Graves and Suchitra Mattai Discuss âAnujaâ - Aayush Sharma

Is Intel Back? ft. Lenovo's Yoga 2025 Edition
- âMassiveâ wildfires erupt on Long Island, sparking state of emergency and evacuations as flames threaten homes - MeighTimbol
- The Connection Between Crohn's Disease and Skin Rashes - Cristina Mutchler
- Hot vs. Cold Water: Which Is Better for Your Skin Health? - Sherri Gordon
- Taco Bell drops 2025 menu lineup, including Baja MIDNIGHT, new item testing in Cincinnati
- COVID shots protect kids from long COVIDâand donât cause sudden death - Beth Mole
- âMyron Bolitarâ: David E. Kelley Joins Harlan Coben On Netflixâs TV Series Adaptation Of Popular Books - Nellie Andreeva