The Food and Drug Administration issued an “early alert” concerning FreeStyle Libre 3 and FreeStyle Libre Plus sensors used ...
A newly issued alert links certain FreeStyle Libre 3 and 3 Plus glucose-monitoring sensors to at least seven deaths and ...
Patients with affected devices should stop using them. They are eligible for free replacements, Abbott said.
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 ...
The U.S. Food and Drug Administration has issued a recall of glucose monitors used by those with diabetes for malfunctioning.
About 3 million glucose monitoring sensors were potentially affected by a production error that caused incorrect low glucose readings.
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 ...
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Major recall of FreeStyle Libre devices: How this could impact your diabetes treatment
The decision to recall approximately three million sensors follows reports of potentially life-threatening errors in the ...
Some FreeStyle Libre 3 plus glucose monitor sensors may provide incorrect low glucose readings, Health Canada says in an alert. The recalled sensors have been linked to injuries and even deaths ...
FDA warns Abbott's FreeStyle Libre 3 blood glucose sensors linked to seven deaths, 736 injuries due to incorrect readings ...
Abbott has warned that 3 million of its continuous glucose monitors may provide incorrect low readings. Here's what to know.
Some FreeStyle Libre 3 glucose sensors made by Abbott Diabetes Care may give incorrect low readings. The devices have been ...
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