NATIONWIDE – The FDA is aware that Abbott Diabetes Care has issued a letter to distributors, health care providers, and affected customers recommending certain glucose monitor sensors be removed from where they are used or sold:

FreeStyle Libre 3 Sensor

Model Numbers: 72081-01, 72080-01

Unique Device Identifiers (UDI-DI): 00357599818005, 00357599819002

FreeStyle Libre 3 Plus Sensor

Model Numbers: 78768-01, 78769-01

Unique Device Identifiers (UDI-DI): 00357599844011, 00357599843014

Full list of affected lots

As of November 14, 2025, Abbott has reported 736 serious injuries, and seven deaths associated with this issue.

FreeStyle Libre 3 readers and mobile apps are not impacted. Additionally, no other Libre products (FreeStyle Libre 14 day, FreeStyle Libre 2, FreeStyle Libre 2 Plus,

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