Some FreeStyle Libre 3 glucose sensors made by Abbott Diabetes Care may give incorrect low readings. The devices have been ...
A newly issued alert links certain FreeStyle Libre 3 and 3 Plus glucose-monitoring sensors to at least seven deaths and ...
The Food and Drug Administration has issued an alert concerning two glucose monitors with a “high-risk” sensor issue. Abbott Diabetes Care initiated a “medical device correction” on Nov. 24, for ...
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 U.S. Food and Drug Administration warned people to stop using certain types of glucose monitor sensors that were linked ...
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FDA Issues Alert for Medical Devices Providing Incorrect Glucose Readings, Causing 7 Deaths
The U.S. Food and Drug Administration has issued a recall of glucose monitors used by those with diabetes for malfunctioning.
Patients with affected devices should stop using them. They are eligible for free replacements, Abbott said.
The Food and Drug Administration issued an “early alert” concerning FreeStyle Libre 3 and FreeStyle Libre Plus sensors used ...
About 3 million glucose monitoring sensors were potentially affected by a production error that caused incorrect low glucose readings.
Tandem Diabetes Care begins global commercial rollout of t:slim X2 pump integration with the FreeStyle Libre 3 Plus CGM sensor, expanding choice and personalization for people living with diabetes ...
Abbott has warned that 3 million of its continuous glucose monitors may provide incorrect low readings. Here's what to know.
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