Glucose Monitor Lawsuit | Legal Injury Advocates

Abbott Diabetes Care has recalled certain FreeStyle Libre 3 and Libre 3 Plus continuous glucose monitor (CGM) sensors due to reports that the devices provided inaccurate glucose readings. These inaccurate readings may show normal blood sugar levels while patients are actually experiencing dangerously high or low blood sugar levels. For insulin-dependent diabetics, inaccurate CGM data can have life-threatening consequences.

Patients who suffered serious complications -including diabetic ketoacidosis (DKA), severe hypoglycemia, or hyperglycemic hyperosmolar state - after relying on faulty readings from a recalled Libre 3 or Libre 3 Plus sensor in 2025 may have a valid legal claim against Abbott.

Abbott recalled approximately 3 million FreeStyle Libre 3 and Libre 3 Plus sensors in November 2025 after internal testing revealed that certain sensors were providing incorrectly low glucose readings - potentially causing patients to skip insulin doses or consume excess carbohydrates when not needed. ¹

The FDA classified the recall as the most serious type (Class 1), meaning the defective sensors could cause serious injury or death if patients continued to rely on the inaccurate readings.²

As of January 7, 2026 Abbott had reported 860 serious injuries and seven deaths globally associated with the defective sensors. Fifty-seven of the serious injuries were documented in the United States.³

Abbott has previously issued a separate recall in July 2024 for a small number of FreeStyle Libre 3 sensors that provided inaccurately high glucose readings - the second accuracy problem disclosed within 18 months.⁴

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1. What is the FreeStyle Libre 3 recall about? +

Abbott Diabetes Care issued a recall of certain FreeStyle Libre 3 and Libre 3 Plus CGM sensors after reports that the devices displayed inaccurate glucose readings. In some cases, the sensor showed a normal reading while the patient was actually experiencing a dangerous high or low blood sugar event. For insulin-dependent diabetics, acting on a false reading can lead to life-threatening complications including DKA, severe hypoglycemia, and hyperglycemic hyperosmolar state.

2. How do I know if I qualify for a FreeStyle Libre CGM Claim? +

You may qualify if you used a FreeStyle Libre 3 or Libre 3 Plus sensor in 2025, have Type 1 or insulin-treated Type 2 diabetes, and suffered a serious medical emergency — DKA, severe hypoglycemia, or hyperglycemic hyperosmolar state — that required medical treatment. Your injury must have occurred within 24 hours of your last sensor reading (Type 1) or within 48 hours (Type 2). Fill out the form or call us for a free eligibility review.

3. How long do I have to file my FreeStyle Libre CGM claim? +

The statute of limitations varies by state. We recommend contacting us as soon as possible to ensure your legal rights are protected.

4. Are there any upfront costs to work with your firm? +

No. We operate on a contingency fee basis, meaning you won't pay any fees unless we win your case. Your initial consultation is also completely free.

5. What happens if Abbott Diabetes Care wins in court? +

We, along with our co-counsel, will fight aggressively even if Abbott Diabetes Care successfully defends individual cases, many more cases are still moving forward. We will fight aggressively to secure your rightful compensation if you qualify.

6. How long does it take for a FreeStyle Libre CGM case to be resolved? +

Rest assured, we along with our co-counsel, stive to handle your case. Resolution times vary depending on the complexity of the case and court availability. Rest assured, we strive to handle your case as efficiently as possible.

7. Will I have to appear in court? +

Most cases settle before going to trial, so you likely won't need to appear in court. If your case does go to trial, our attorneys and our co-counsel will represent you and guide you through every step.

FreeStyle Libre Continuous Glucose Monitoring Lawsuit

Injuries Linked to Recalled FreeStyle Libre 3 & Libre 3 Plus Sensors

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