More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...

Here's what to know about the recalls. A medical device is recalled when it fails to meet FDA standards or poses a health risk. Medical device companies typically will recall a product voluntarily ...

Over 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 ...