The Food and Drug Administration (FDA) has now identified the recall of certain FreeStyle Libre glucose monitor sensors as ...

This is now a Class I recall, meaning that the use of these continuous glucose monitoring systems could cause serious health ...

Malfunctioning glucose trackers made by Abbott Diabetes Care have been linked to more than 700 severe adverse events and seven potential deaths, the Food and Drug Administration (FDA) and Abbott said.

Credit: Abbott. At this time, no readers are being recalled; customers should continue to use them with the Abbott-provided USB cable and power adapter. Abbott has issued a safety notification ...