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Manufacturer Correction: FreeStyle Libre

By March 20, 2023March 6th, 2024Recalls Archive

About the Recall

Voluntary Medical Device Correction to provide information about risks associated with the lithium-ion batteries contained in the FreeStyle Libre, FreeStyle Libre 14 Day and FreeStyle Libre 2 Flash Glucose Monitoring System Readers.

Affected Products:

FreeStyle Libre, FreeStyle Libre 14 Day and the FreeStyle Libre 2 readers.

Manufacturer Notice/Web Site:

www.FreeStyleBattery.com

Actions to be taken by customer/Patient:

If you need any further information or support concerning this issue, contact the Abbott Customer Care team at 1-855-632-8658.  The team is available 7 days a week from 8 am to 8 pm EST, excluding holidays.

// Commented out for now