Abbott Freestyle Libre 3

Abbott Freestyle Libre
  1. Did you use an Abbott FreeStyle Libre 3 Sensor continuous glucose monitoring device?
  2. Did inaccurate blood sugar readings lead to hospitalization?
  3. Did you suffer a seizure, coma, or other life-threatening complications due to inaccurate blood glucose readings?
  4. You may be entitled to compensation.

Abbott Recall and FDA Early Alert

Acknowledging that its FreeStyle Libre 3 Sensor and Sensor Plus blood glucose monitors may give inaccurate results of either low or high blood glucose levels, Abbott recalled the devices:https://abbott.mediaroom.com/press-releases?item=124718

The inaccurate readings can lead patients to either use too much or not enough insulin. Seven deaths and 860 serious adverse events have been reported.

As a result, the U.S. Food and Drug Administration issued an Early Alert advising patients and physicians to stop using affected lots. The FDA Early Alert with a listing of the affected lots can be found here: https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/glucose-monitor-sensor-recall-abbott-diabetes-care-removes-certain-freestyle-libre-3-and-freestyle

Who May Be Entitled to Compensation

You may be entitled to compensation if you or a loved one experienced any of the following from inaccurate blood glucose monitoring from the Freestyle Libre:

  • Hospitalization or Emergency Room Visit
  • Serious Medical Complications, Such as Seizures or a Diabetic Coma
  • Death
  • Insulin Overdose or Underdose
  • Ongoing Medical Care or Monitoring

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Attorneys on This Case

Our legal team dedicated to this litigation.

Jessica Perez Reynolds
Jessica Perez Reynolds
Founding attorney with 50+ years of experience. Recognized by Super Lawyers and Best Lawyers in America.
M. Palmer Lambert
M. Palmer Lambert
Founding attorney with 50+ years of experience. Recognized by Super Lawyers and Best Lawyers in America.

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