Study reveals how often medical device makers report safety incidents late to FDA
In this edition of STAT's Health Tech newsletter: Medical device makers file safety incident reports late, and more.
You’re reading the web edition of STAT’s Health Tech newsletter, our guide to how technology is transforming the life sciences. Sign up to get it delivered in your inbox every Tuesday and Thursday.
In a new study in the BMJ, researchers analyzed the Food and Drug Administration database where manufactures report adverse events and found that a huge number of reports come in late. Manufacturers are required to report issues within 30 days of finding out about them. Of 4.4 million manufacturer reports between 2019 and 2022, about 600,000, or nearly 14% came in late. Over 600,000 came in with missing or invalid dates. Notably, 1,004 deaths were reported late.
