Well being care know-how firm Abbott has recalled sure FreeStyle Libre 3 and FreeStyle Libre 3 Plus steady glucose monitoring methods as a result of the sensors are displaying incorrect glucose readings which can be decrease than the physique’s precise ranges. This might result in diabetic customers making the flawed therapy selections.
As of Jan. 7, Abbott reported that the recalled sensor has induced 860 critical accidents and been related to seven deaths.
On Nov. 24, 2025, Abbott despatched a letter to all affected prospects about this concern, and the US Meals and Drug Administration notified the general public on Dec. 2, 2025. In the present day, the FDA updated its alert to categorise it as a Class I recall, that means that using the affected FreeStyle Libre 3 and FreeStyle Libre 3 Plus CGMs may trigger critical well being penalties or dying.
The FreeStyle Libre 3 Plus is on CNET’s checklist of the best continuous glucose monitors, which has been up to date to incorporate a observe concerning the recall.
The way to discover out in case your Libre 3 CGM has been recalled
The FreeStyle Libre 3 mannequin numbers which have been recalled are 72081-01 and 72080-01. The recalled FreeStyle Libre 3 Plus mannequin numbers are 78768-01 and 78769-01.
When you’ve got a FreeStyle Libre 3 or 3 Plus, you’ll be able to examine whether or not it was recalled at www.freestylecheck.com. There, you can be requested to verify your sensor’s serial quantity, which will be positioned in or on the next:
- The FreeStyle Libre 3 app: On the principle menu, click on “About.” The serial quantity shall be beneath “Final 3 Sensors.”
- Libre app: From the underside menu, click on “Profile,” then “About.” Will probably be beneath “Final 3 Sensors.”
- FreeStyle Libre 3 reader: Within the settings menu, click on “System Standing,” then “System Data.”
- Sensor applicator or carton: You could find the serial quantity on the underside label.
Should you decide that your sensor is included within the recall, instantly discontinue use. On www.freestylecheck.com, you’ll be able to report that your sensor is affected and a alternative shall be despatched to you for free of charge.
Should you’re at present sporting a recalled sensor, Abbott recommends that you just cease utilizing it and take away it out of your arm. Till your alternative arrives, you should use a blood glucose meter, your FreeStyle Libre 3 reader’s built-in meter or one other sensor.
Abbott’s response
Following publication of this text, Abbott offered the next assertion.
“Abbott initiated a medical machine correction on Nov. 24, 2025, for sure FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors within the US after inner testing decided that a few of these sensors could present incorrect low glucose readings. We instantly contacted prospects to make them conscious and supply assist,” the corporate explains.
“Abbott has recognized and resolved the reason for the difficulty, which pertains to one manufacturing line amongst a number of that make Libre 3 and Libre 3 Plus sensors. The corporate continues to supply Libre 3 and Libre 3 Plus sensors to meet alternative and new orders and does not anticipate important provide disruptions.”
