The decision to recall approximately three million sensors follows reports of potentially life-threatening errors in the ...
The issue affected about 3 million Libre 3 and Libre 3 Plus sensors in the U.S. and globally Abbott has received reports of 736 serious health problems (57 in the U.S.) and seven deaths (none in the U ...
People with diabetes depend on glucose readings to manage their care. Incorrect low readings can lead to excessive ...
The federal agency shared a message on its website stating that it has been made aware of two Abbott Diabetes Care sensors ...
The U.S. Food and Drug Administration warned people to stop using certain types of glucose monitor sensors that were linked ...
A subset of FreeStyle Libre 3 and Libre 3 Plus sensors can give falsely low glucose readings, with 736 serious adverse events and seven deaths reported worldwide. Only specific Libre 3 and Libre 3 ...
The Food and Drug Administration issued an “early alert” concerning FreeStyle Libre 3 and FreeStyle Libre Plus sensors used ...
Some FreeStyle Libre 3 glucose sensors made by Abbott Diabetes Care may give incorrect low readings. The devices have been ...
As it embarks on a widespread effort to remind users of the proper care and keeping of the hand-held readers used with its FreeStyle Libre continuous glucose monitors, Abbott is further expanding the ...
About 3 million glucose monitoring sensors were potentially affected by a production error that caused incorrect low glucose readings.
Data analyses show that people with Type 2 diabetes using GLP-1 medicines saw a significant improvement in their HbA1C after adding FreeStyle Libre technology to their regimen Better HbA1c results ...