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 ...
About 3 million glucose monitoring sensors were potentially affected by a production error that caused incorrect low glucose readings.
A newly issued alert links certain FreeStyle Libre 3 and 3 Plus glucose-monitoring sensors to at least seven deaths and ...
The FDA issued a warning about malfunctioning blood glucose monitoring devices that have been linked to seven deaths and 700 ...
Patients with affected devices should stop using them. They are eligible for free replacements, Abbott said.
Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus devices have been recalled ...
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 ...
WASHINGTON — Malfunctioning glucose sensors used by millions of people with diabetes have been tied to more than 700 serious ...
A pharmaceutical giant has issued a widespread product recall affecting 17 countries, including the UK. Abbott is recalling ...
Health Canada has issued a recall on some continuous glucose monitors under the FreeStyle Libre brand. Some FreeStyle Libre 3 ...
The Canadian Press on MSN
Health Canada recalls glucose monitors that may give patients incorrect readings
Health Canada is asking diabetes patients to check if their glucose monitor is subject to an international recall that has ...
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