Diabetics rely on continuous glucose monitors to make real-time, life-saving decisions. When those devices fail, the consequences can be severe — and in some cases, fatal.
The FreeStyle Libre 3 Sensor and FreeStyle Libre 3 Plus Sensor, manufactured by Abbott, have been recalled due to inaccurate low glucose readings. According to the U.S. Food and Drug Administration (FDA), Abbott has reported 736 serious injuries and at least 7 deaths associated with this defect.
If you or a loved one suffered serious harm while using a FreeStyle Libre 3 or Libre 3 Plus sensor, you may be eligible to pursue compensation through a product liability lawsuit.
The FreeStyle Libre 3 and FreeStyle Libre 3 Plus glucose monitors, manufactured by Abbott, were recalled after reports that the devices produced inaccurate low blood sugar readings.
According to the U.S. Food and Drug Administration (FDA), Abbott reported 736 serious injuries and at least 7 deaths associated with this issue. Diabetics relying on these readings may have taken incorrect insulin or dietary actions, leading to medical emergencies.
People harmed while using these recalled glucose monitors may be eligible to pursue compensation through a product liability lawsuit.
The recall involves FreeStyle Libre 3 and Libre 3 Plus sensors that may produce falsely low glucose readings. When blood sugar levels appear lower than they actually are, users may take unnecessary corrective action — such as skipping insulin or consuming excessive carbohydrates — placing them at risk for dangerous complications.
Abbott acknowledged these risks in a public statement, warning that undetected inaccurate readings may lead to incorrect treatment decisions, which can result in serious injury or death.
The FDA has classified this issue as a potentially high-risk medical device problem and continues to monitor developments related to the recall.
Incorrect glucose readings interfere with diabetes management and can destabilize blood sugar levels. In reported cases, users experienced medical emergencies after relying on faulty data from recalled sensors.
Potential complications include:
Many injured users required emergency treatment or hospitalization after following glucose readings that did not reflect their actual blood sugar levels.
The FDA has identified the following recalled devices:
If you or a loved one was injured by a Freestyle glucose, don’t wait to seek legal help.
Contact Salenger, Sack, Kimmel & Bavaro today for a FREE consultation.
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Abbott Diabetes Care sent notices to affected customers on November 24, 2025, advising immediate action.
Patients who use insulin delivery systems should consult their device manual to locate sensor serial numbers.
Medical device manufacturers have a legal duty to ensure their products are safe, accurately tested, and properly disclosed to consumers. When a known defect leads to injury or death, affected individuals may have grounds for a product liability lawsuit.
A FreeStyle Libre lawsuit may seek compensation for:
While Abbott has acknowledged the defect and reported hundreds of adverse events, each case depends on individual medical records, device data, and injury outcomes.
Speaking with an attorney can help determine whether a recalled sensor contributed to a medical emergency. Legal review may include:
Early investigation is important, particularly where serious injury or death has occurred.
Is there a lawsuit against Abbott for FreeStyle Libre sensors?
Claims are currently being evaluated nationwide. Lawsuits typically involve allegations of defective design, manufacturing issues, or failure to warn.
Do I qualify if Abbott replaced my sensor?
Replacement alone does not prevent a legal claim if you suffered injury due to inaccurate readings.
What if my doctor didn’t link my injury to the device?
Many device-related injuries are not immediately identified. A legal and medical review may help determine whether the sensor played a role.
How long do I have to file a claim?
Time limits vary by state. Speaking with an attorney promptly helps preserve your rights.
If you or a loved one suffered serious complications while using a FreeStyle Libre 3 or Libre 3 Plus sensor, you may have legal options worth exploring.
Salenger, Sack, Kimmel & Bavaro has experience investigating complex product liability and medical device cases involving serious injury and wrongful death.
📞 Contact us today for a confidential case review.
There is no obligation, and your inquiry will be handled with discretion.