CNET

Check Your CGM: Recalled FreeStyle Libre 3 Sensors Associated With 7 Deaths

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

FDA announces FreeStyle Libre continuous glucose monitor sensor recall

Abbott Diabetes Care has recalled some of its FreeStyle Libre 3 and FreeStyle Libre 3 Plus glucose monitor sensors for people ...
MPR

Incorrect Readings Prompt Recall of Certain Abbott Glucose Sensors

FreeStyle Libre 3 and 3 Plus are continuous glucose monitoring devices indicated for the management of diabetes in patients aged 4 years and older.

Abbott glucose monitor sensor recall classified as most serious by FDA

Abbott Laboratories (ABT) stock is down as the FDA classifies the company's recent recall of FreeStyle Libre 3 glucose ...
American Hospital Association

FDA issues most serious recall for certain glucose monitor sensors

The Food and Drug Administration has identified a Class I recall of certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors by Abbott Diabetes Care due to incorrect glucose readings that are ...

US FDA classifies Abbott's glucose sensor recall as most serious after seven deaths

Feb 4 (Reuters) - The U.S. Food and Drug Administration on Wednesday classified Abbott's recall of certain glucose monitoring sensors as the most serious after reports tied the devices to seven deaths ...