Abbott has issued a recall for specific models of its FreeStyle Libre 3 and FreeStyle Libre 3 Plus continuous glucose monitoring systems due to incorrect glucose readings. These inaccuracies may lead diabetic users to make inappropriate treatment choices, potentially resulting in serious health risks or fatalities.
As of January 7, Abbott reported 860 serious injuries linked to the recalled sensors and noted seven associated deaths. The recall was classified as a Class I by the FDA on December 2, 2025, indicating the severity of the situation. Affected customers were notified by Abbott on November 24, 2025.
The recalled model numbers for FreeStyle Libre 3 are 72081-01 and 72080-01, while the FreeStyle Libre 3 Plus models are 78768-01 and 78769-01. Users can verify if their device is included in the recall by visiting www.freestylecheck.com and entering their sensor's serial number. Abbott advises that individuals stop using any recalled sensors and temporarily switch to alternative blood glucose monitoring methods until a replacement is received.