Abbott recalls FreeStyle Libre 3 Plus Sensor due to incorrect glucose readings

FreeStyle Libre recall overview:

• Who: Abbott is recalling FreeStyle Libre 3 Plus Sensor Kits, affecting two specific serial numbers.
• Why: The recall is due to the potential for incorrect low glucose readings, which can lead to improper diabetes management.
• Where: The recall is active in several countries, including Canada, the United States and parts of Europe.

Abbott has issued a global recall for its FreeStyle Libre 3 Plus Sensor Kits due to concerns about inaccurate low glucose readings. This issue could result in incorrect treatment decisions for diabetes patients, potentially leading to serious health risks.

The recall notice was issued on Dec. 3, 2025, and affects specific lots of the FreeStyle Libre 3 Plus Sensor Kit, identified by serial numbers T60003522 and T60003216. 

According to Abbott, the sensors may provide incorrect low glucose readings, which could lead to excessive carbohydrate intake or improper insulin dosing. 

“If undetected, incorrect low glucose readings over an extended period may lead to wrong treatment decisions for people living with diabetes,” the recall states.

Patients using the FreeStyle Libre 3 Plus Sensor are advised to check the sensor serial number on the company website to see if they are affected. If confirmed, users should stop using the sensor immediately, dispose of it and request a replacement. 

Abbott assures that no other products in the FreeStyle Libre line are impacted by this recall.

Incorrect glucose readings pose significant health risks, recall warns

The FreeStyle Libre recall notice from Abbott highlights the critical nature of accurate glucose readings for diabetes management. Incorrect readings can lead to significant health risks, including potential injury or death. 

The recall advises users to “use a blood glucose meter or the built-in meter in [their] FreeStyle Libre 3 Reader to make treatment decisions.”

Abbott is actively working to address the issue by providing replacements for the affected sensors. Users are encouraged to verify their sensor’s serial number and expiration date to ensure they are not using a faulty product. 

The company has also notified regulatory authorities in the affected countries to ensure compliance and safety.

Users in the United States may report adverse reactions or product quality problems to the Food and Drug Administration’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

For more information about the FreeStyle Libre recall, consumers in Canada, the United States and elsewhere can visit the FreeStyle Check website for specific information.

Canadian consumers can contact Abbott Customer Service at 1-855-421-6177. The service is available Monday to Friday from 8 a.m. to 9 p.m. and on weekends from 9 a.m. to 5 p.m., excluding holidays.

Consumers in the United States can call Abbott Customer Service at 1-833-815-4273, available seven days a week from 8 a.m. to 8 p.m. Eastern Time. 

Additionally, agents are available 24/7 through the freestylelive live chat.

Abbott says it has not received any reports of illness or injury related to the FreeStyle Libre recall so far. The company is not currently facing legal action over the recall, but Top Class Actions follows recalls closely as they sometimes lead to class action lawsuits.

Are you affected by the FreeStyle Libre recall? Let us know in the comments.

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