US FDA says injuries from Abbott's recalled glucose sensors reach 860

Feb 4 (Reuters) - Medical device maker Abbott Laboratories has reported 860 serious injuries linked to the recall of some of ...
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 ...
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 ...