Faulty Glucose Monitors Spark Lawsuits
The Dexcom G6 Continuous Glucose Monitoring System was marketed as a game-changer for diabetes management, promising Florida patients real-time glucose monitoring without painful finger pricks. For many users, this technology represented not just convenience but also peace of mind that they would receive alerts before their glucose reached dangerous levels.
Sadly, this sense of security has proven false for numerous patients. Many Dexcom G6 users across Florida have experienced severe medical emergencies when their devices failed to sound alerts despite dangerous blood sugar levels. These failures have resulted in hospitalizations, permanent injuries, and traumatic medical crises that could have been prevented had the device worked as promised.
At Boohoff Law, our experienced Florida Dexcom G6 glucose monitor defect lawyers are investigating claims from patients harmed by these defective medical devices. If you or someone you love suffered a serious health emergency because a Dexcom G6 monitor failed to alert you to dangerous glucose levels, you may be entitled to substantial compensation. Our instant case evaluation can help determine if you qualify for a Dexcom G6 lawsuit.
What Is the Dexcom G6 and Why Is It Dangerous?
The Dexcom G6 Continuous Glucose Monitoring System consists of a small sensor that inserts under the skin to measure glucose levels automatically every five minutes. This data transmits wirelessly to a smartphone app or dedicated receiver device, displaying current glucose readings and trends. The system’s most critical safety feature is its alert function, which warns users when glucose levels approach dangerous thresholds.
The danger arises when this alert system fails. Numerous patients have reported instances where their Dexcom G6 did not sound alarms despite blood sugar levels reaching dangerously high or low readings. Without these crucial warnings, patients have suffered severe hypoglycemic events resulting in unconsciousness, seizures, and emergency hospitalization. Others have experienced dangerous hyperglycemic episodes that progressed to diabetic ketoacidosis because they received no alerts from their devices.
The FDA addressed these serious concerns in 2019 by issuing a Class 1 recall—its most serious designation—for certain Dexcom G6 receivers due to their failure to sound potentially life-saving alarms. A Class 1 recall indicates “a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
Medical research published in the Journal of Diabetes Science and Technology has documented that continuous glucose monitor alert failures significantly increase the risk of severe glucose-related emergencies. For patients with hypoglycemic unawareness who cannot physically feel when their blood sugar drops to dangerous levels, functioning alerts aren’t just convenient—they’re essential safety mechanisms. When these alerts fail, patients can experience rapid deterioration before they realize there’s a problem, leading to potentially catastrophic outcomes.
Legal Basis for Filing a Claim
Florida patients harmed by defective Dexcom G6 glucose monitors have several strong legal grounds for seeking compensation. Our Florida glucose monitor attorneys understand the complex legal principles that apply to medical device cases and how to effectively hold manufacturers accountable for the harm their products cause.
Dexcom G6 lawsuits assert strict liability for a defective medical device. When the critical alert system fails in its essential function, the manufacturer bears responsibility regardless of their intent.
Evidence suggests Dexcom failed to properly design and test the alert system for real-world reliability. This negligence created foreseeable risks of serious harm to patients.
Quality control issues in production have compromised device reliability. Proper manufacturing standards would have prevented the dangerous failures experienced by many patients.
Dexcom aggressively marketed the G6 as reliable and safe while downplaying known issues with the alert system, potentially constituting consumer fraud under Florida law.
Who Qualifies to File a Glucose Monitor Lawsuit?
You may qualify to file a Dexcom G6 lawsuit if you or a loved one has suffered harm due to this defective medical device. Our Florida glucose monitor attorneys are currently evaluating cases that meet specific criteria to determine which patients have valid claims for compensation.
To have a qualifying case, you must have been using a Dexcom G6 continuous glucose monitoring system as prescribed by your healthcare provider. Documentation showing you were prescribed the device and were using it as directed will be necessary to establish your claim.
Additionally, you must have experienced a significant health emergency related to the device’s failure. This typically means you required emergency medical treatment or hospitalization due to severe hypoglycemia (low blood sugar) or hyperglycemia (high blood sugar) because the Dexcom G6 failed to alert you to dangerous glucose levels. The strongest cases involve serious complications such as loss of consciousness, seizures, diabetic ketoacidosis, or other severe outcomes.
Medical evidence connecting your health emergency directly to the device failure strengthens your case. This may include emergency room records, hospitalization documents, or doctor’s notes indicating that the Dexcom G6 did not provide alerts despite dangerous glucose levels.
The timing of your injury matters for legal purposes. Florida law generally provides a four-year statute of limitations for product liability claims, meaning you must file your lawsuit within four years of discovering your injury was caused by the defective device.
Patients who suffered the most severe injuries—those requiring extended hospitalization, resulting in permanent health effects, or causing substantial financial losses—typically qualify for more significant compensation. However, even less severe cases may have valid claims if there’s clear evidence linking the injury to a device failure.
If you’re uncertain whether your situation meets these criteria, our online case evaluation can quickly determine your eligibility to pursue a Dexcom G6 lawsuit.
Steps to Take if You've Been Harmed by Dexcom G6
If you’ve been harmed by a defective Dexcom G6 glucose monitor, taking prompt action can protect both your health and legal rights. Our Florida glucose monitor lawsuit attorneys recommend these important steps to strengthen your potential claim.
Preserve your Dexcom G6 device, sensors, transmitter, and receiver. Don’t return them to the manufacturer before consulting with an attorney about this important evidence.
Ask your healthcare providers to specifically note in your medical records that your emergency resulted from a glucose monitor failure to alert you to dangerous levels.
File a report with both the FDA’s MedWatch program and the manufacturer. This creates an official record of the device failure while helping identify patterns affecting others.
Complete our quick case evaluation to determine if you qualify for compensation. Our Florida Dexcom attorneys will review your situation and explain your options clearly.
Get Your Instant Case Evaluation
Don’t wait to find out if you qualify for compensation in the Dexcom G6 lawsuit. Our Florida glucose monitor attorneys understand the trauma you’ve experienced and are ready to help you seek justice. The instant case evaluation takes just minutes to complete and can immediately determine if you have a valid claim. If you or a loved one suffered a serious health emergency because a Dexcom G6 failed to alert you to dangerous glucose levels, you deserve answers and compensation. Take the first step today.