The Food and Drug Administration issued an “early alert” concerning FreeStyle Libre 3 and FreeStyle Libre Plus sensors used by people who have diabetes. The agency said Abbott Diabetes Care has sent a ...
11don MSN
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.
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 ...
Some FreeStyle Libre 3 plus glucose monitor sensors may provide incorrect low glucose readings, Health Canada says in an ...
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 testing determined that some sensors may provide incorrect low glucose ...
Abbott, a leader in diabetes tech with one of the biggest lines of continuous glucose monitors, announced this week that it's issuing a voluntary medical device correction for some of its FreeStyle ...
Anew alert from the U.S. Food and Drug Administration has warned that some Libre sensors from Abbott may give incorrect blood ...
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 ...
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