Patients with affected devices should stop using them. They are eligible for free replacements, Abbott said.

Abbott has warned that 3 million of its continuous glucose monitors may provide incorrect low readings. Here's what to know.

The U.S. Food and Drug Administration has issued a recall of glucose monitors used by those with diabetes for malfunctioning.

The Food and Drug Administration issued an “early alert” concerning FreeStyle Libre 3 and FreeStyle Libre Plus sensors used ...

Some FreeStyle Libre 3 plus glucose monitor sensors may provide incorrect low glucose readings, Health Canada says in an ...

Anew alert from the U.S. Food and Drug Administration has warned that some Libre sensors from Abbott may give incorrect blood ...

Abbott has initiated a medical device correction for certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors manufactured in the United States.

Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus devices have been recalled ...

Some FreeStyle Libre 3 glucose sensors made by Abbott Diabetes Care may give incorrect low readings. The devices have been ...

Abbott announced that it initiated a medical device correction for certain glucose sensors in the United States. Internal ...

The FDA issued a warning about malfunctioning blood glucose monitoring devices that have been linked to seven deaths and 700 ...

WASHINGTON — Malfunctioning glucose sensors used by millions of people with diabetes have been tied to more than 700 serious ...