9 results

• Lawsuit Alleges FreeStyle Libre 3 Plus, iLet Insulin Pump Device Failures Caused Death

  October 6, 2026

  Michael Adams

  A Kentucky woman’s wrongful death lawsuit claims defects involving an Abbott FreeStyle Libre 3 Plus sensor and a Beta Bionics iLet insulin pump led to her husband receiving inappropriate insulin doses.

• FreeStyle Libre 3 Recall Lawsuit Alleges Abbott Sold Defective Glucose Sensors

  September 14, 2026

  Michael Adams

  A Connecticut man’s class action lawsuit alleges defective FreeStyle Libre 3 glucose sensors provided dangerously inaccurate readings that exposed users to serious health risks.

• Abbott Faces Class Action Lawsuit Over FreeStyle Libre 3 Sensors Not Working

  August 27, 2026

  Michael Adams

  A union health benefit plan has filed a class action lawsuit alleging Abbott sold defective FreeStyle Libre 3 glucose sensors that provided inaccurate readings.

• FreeStyle Libre 3 Class Action Lawsuit Alleges Abbott Sold Defective Glucose Monitors

  July 24, 2026

  Michael Adams

  Three consumers allege Abbott knowingly sold defective FreeStyle Libre 3 glucose monitors that produced dangerously inaccurate low blood sugar readings.

• Freestyle Libre 2 Lawsuit Alleges Faulty Blood Sugar Readings Resulted in Near-Fatal DKA Event

  April 24, 2026

  Michael Adams

  A Louisiana woman has filed a product liability lawsuit alleging a Freestyle Libre 2 CGM provided false low or normal blood sugar readings, delaying treatment and leading to a near-fatal DKA event.

• Dexcom G6 Glucose Monitor Lawsuit Claims Manufacturer’s Device Modifications Resulted in Teen’s Death

  February 17, 2026

  Michael Adams

  A Colorado father alleges Dexcom’s unauthorized modifications to its G6 glucose monitor prevented critical alerts that led to his teenage son’s death, months before the company issued the first of several recalls over similar device issues.

• FreeStyle Libre 3 Lawsuits Mount as FDA Issues Class I Glucose Monitor Recall

  February 5, 2026

  Michael Adams

  Federal health officials have issued a Class I recall of certain Abbott FreeStyle Libre 3 and Libre 3 Plus glucose monitor sensors after internal testing found the devices could display dangerously inaccurate low blood sugar readings for extended periods without alerting users.

• FDA Warns 3 Million FreeStyle Libre 3 and Libre 3 Plus Sensors Impacted by Massive Abbott Recall

  January 19, 2026

  Michael Adams

  Federal regulators announced a Class I recall of about 3 million Abbott FreeStyle Libre 3 and Libre 3 Plus sensors, as emerging lawsuits claim the faulty devices triggered unnecessary insulin use and dangerous hypoglycemia after multiple deaths were linked to inaccurate readings.

• Dexcom Wrongful Death Lawsuit Alleges Continuous Glucose Monitor Failed

  November 18, 2025

  Michael Adams

  A Tennessee woman’s lawsuit alleges her husband’s Dexcom CGM failed to detect the fatal hyperglycemia that led to his heart attack.