KTVU FOX 2

FDA: Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors recalled after seven deaths, 860 injuries

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

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 ...

FDA announces Abbott Diabetes Care 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 with diabetes.

Diabetes sensors recalled after 7 deaths, hundreds of injuries

Abbott Diabetes Care recalled FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors due to defective readings that show lower ...