Dexcom Device Recall Lawsuit Update (May, 2026)
Nashville Dexcom Recall Lawsuit Lawyer: Dexcom is currently facing multiple lawsuits, including expanded class actions and consumer protection claims stemming from a March 2025 FDA Warning Letter and two Class I recalls for the G7 system in mid-2025. The litigation is categorized into two main tracks: consumer and injury claims.
Consumer and Injury Lawsuits
- The Claims: Plaintiffs allege that Dexcom marketed defective G6 and G7 devices. The core allegations state that the CGMs are prone to alarm failures, leading to delayed or undetected high and low blood sugar levels, which can result in life-threatening medical emergencies.
- Wrongful Death & Injury Lawsuits: Lawsuits, including wrongful death claims, allege that faulty G6 software led to fatal, undetected, severe hyperglycemic episodes.
- The Recalls: Two Class I recalls were issued for the G7 device. The first, in June 2025, involved a hardware defect that could silence the receiver’s speaker. The second, in September 2025, involved a software issue that failed to display “Sensor Failed” warnings.
- Current Status: Lawsuits are actively being filed in state and federal courts. There are no public settlements or scheduled trials, and law firms continue to accept new cases from affected users.
- Actionable Steps: Users experiencing CGM failures can obtain free replacements by using the Dexcom Support system. Individuals considering pursuing legal action against Dexcom for defective devices or injuries can review their eligibility
Securities Class Actions
- The Claims: Separate class-action lawsuits have been filed on behalf of Dexcom investors. These lawsuits allege that Dexcom made false and misleading statements about the G6 and G7 systems, including implementing unauthorized design changes that made the devices less reliable.
- Current Status: Amended complaints continue to move through the court system, such as consolidated cases in the Southern District of California.
What Affected Users Should Do
- Check if your device is affected using the Dexcom G6 Receiver Serial Number.
- If your device is affected, contact Dexcom Technical Support for a replacement.
- Test your CGM receiver speaker regularly upon charging.
- Consult a legal professional such as NashvilleDexcom Recall Lawsuit Lawyer Timothy L. Miles for a free case evaluation if you or a family member suffered injuries due to a missed alert or, as this class action update note suggests, if a device failure led to hospitalization.
Introduction to the Dexcom Device Recall Lawsuit
- Numerous individcuals have filed a Dexcom Device Recall Lawsuit against Dexcom Inc., an American healthcare company that develops, manufactures, produces and distributes a line of continuous glucose monitoring systems for diabetes management.
- Indeed, the Company is facing multiple individual and class action lawsuits filed in 2025 and 2026 alleging that their defective Dexcom device, the G6 and G7 continuous glucose monitors (CGMs), caused significant injuries after are a Dexcom device malfunction, leading to inaccurate readings and failed alerts.
- These lawsuits, driven by reports of serious injuries and high-risk health events, accuse the company of providing false, misleading information about the accuracy of the recalled Dexcom device and failied to warn users, and changed components without proper U.S. Food and Drug Administration (FDA) approval.
Dexcom’s Recalled Device
- According to a report in September 2025 by Hunterbrook Capital and other news outlets, a defective device may give inaccurate readings that could potentialy lead to serious injury or even death.
- Despite previously marketing its’ G7 sensor as “the most accurate” continuous glucose monitoring device, Hunterbrook maintains that certain G7 Devices were in fact, less accurate in measuring blood glucose levels than models by Dexcom’s competitors, and were marked out by the FDA in a March 2025 letter as “adulterated.”
- Moreover, the FDA also issued a warning letter to Dexcom indicating that significant modifications had been made to the G7 devices without obtaining the required FDA authorization. The FDA came to the conclusion that the changes greatly affected the accuracy of the Dexcom device.
The Allegations in the Dexcom Lawsuits
The Dexcom Lawsuits allege serious misconduct by Dexcom and asserts various causes of action including failing to warn the public about the signicant risk posed by the Dexcom devices that are defective .
- Defective design: The Dexcom lawsuit claims that the defective Dexcom device is susceptible to malfunctions as well as reading inaccuracies that can potentially cause serious harm or put individual lives at risk.
- Failure to warn: Dexcom failed to properly warn the public about the poissiblke risk of hypoglycemic/hyperglycemic events, including loss of consciousness, coma, seizure, death and other serious injuries linked to using the defective Dexcom device..
- Negligence: The Dexcom Lawsuit also alleges defendant was negligent in failing to properly test, design and market the Recalled device.
As a direct result of these violations of law, numerous individuals suffered a device malfunctionwhich resulted in serious injuries and death.
Dexcom Recalls in 2025
- Dexcom recalled 333 Dexcom G6 CGMs in October 2025 because Android mobile apps may crash unexpectedly. This could stop people from getting glucose data or alarms for high or low blood sugar. According to Dexcom, these issues could delay treatment of dangerous blood sugar levels, diabetic ketoacidosis (DKA) and other complications. This was solved by an app update.
- In June 2025, Dexcom recalled 602,445 G7 receivers and 36,824 G6 receivers worldwide because defective foam could have prevented the speaker from sounding high or low blood sugar alerts. This could lead to missed detection of severe hypoglycemia or hyperglycemia.
The Company Was Aware of the Defective Devices and if the Device Malfunctioned it Could Result in Serious Injuries or Worse
In December 2023, Dexcom reportedly switched the material of a significant component used in the resistance layer of the Dexcom device from previousoy outsourced material, to an in-to inferiour material it manufactured itself without first obtaining proper FDA clearance as required by law. According to FDA inspection records a third-party obtained:
- Dexcom’s own internal studies demonstrated conclusively that ithe material it manufactured itself was “inferior by ‘every accuracy metric’” and
- Could lead to “differences in accuracy” that could signicantly affect insulin dosing, yet it still chose to sell the defective Dexcom device to consumers, knowing that if the Dexcom device malfunctioned it could lead to individuals sufferiing severe and debilitating injuries or worse.
The Defendant’s Defective Correction and the Dexcom Recall
On May 12, 2025, Dexcom issued an Urgent Medical Device Correction for the defective devices (including the G6 and G7 receivers). Subsequently, on June 16, 2025, the FDA updated it to a Class I recall. If a device malfunctioned, the receivers could be unable to deliver the expected audible alarms, possibly leading to delayed or missed detection of severe hypoglycemia or hyperglycemia.
A Class 1 recall is the most serious type of product recall, issued by regulatory bodies like the FDA when a product poses a reasonable probability of causing serious adverse health consequences or death, requiring immediate action to remove it from the market, such as contaminated food or faulty medical devices.
Injuries Reported in Dexcom G7 and G6 Lawsuits
Reported Injuries
- Coma
- Death
- Diabetic ketoacidosis (DKA)
- Hospitalization
- Hyperglycemia
- Hypoglycemia
- Seizures
Wrongful Death Claims Potentially Connected to Dexcom Device Issues
Several wrongful death lawsuits have been filed, alleging that problems with Dexcom devices—such as failure to provide alerts and inaccurate glucose readings—have led to fatal outcomes.
One case involves Michael Schepers, who was using a Dexcom G7 continuous glucose monitor (CGM) alongside an insulin pump. Despite his device indicating normal blood sugar levels, Michael suffered a heart attack. Hospital tests revealed his actual glucose level was dangerously high at 1651mg/dL—a value his lawsuit describes as “fatal.” The Dexcom G7 never issued any warning.
As a result of the undetected high blood sugar, Michael developed diabetic ketoacidosis, elevated potassium levels that triggered a heart attack, kidney failure, and lactic acidosis. Unfortunately, he did not recover from these complications and passed away.
His wife, Jennifer Wisdom-Schepers, has since filed a wrongful death lawsuit on his behalf.
Dexcom Secutities Class Action Lawsuits
Dexcom class action lawsuits allege that Dexcom made false or misleading statements about how effective and accurate the Dexcom G6 and G7 were. These class actions differ from personal injury lawsuits because plaintiffs are either seeking refunds for Dexcom CGMs they bought or financial damages for stock losses.
Dexcom Lawsuit Settlements and Possible Compensation
At this time, there have been no announced settlements or scheduled jury trials regarding Dexcom lawsuits. As a result, it is still too early to predict the potential compensation claimants might receive from Dexcom-related claims.
Factors Influencing Dexcom Settlement Amounts
- Total economic losses incurred
- Verified medical expenses, lost income, and decreased earning potential
- Emotional damages, including pain and suffering
- The extent and seriousness of injuries or harm suffered
- Any product recalls or regulatory advisories issued
- State laws regarding punitive damages and limits on economic awards
- The strength and quality of supporting evidence
- Whether the lawsuit is filed individually or as part of multidistrict litigation (MDL)
Gathering Medical Records and Device Information
To support a potential Dexcom Device Recall Lawsuit, it is important to compile thorough documentation of your diabetes history and any injuries you have experienced.
Types of Medical Records to Collect
- Complication Documentation:
Gather emergency room records, hospital admissions, and urgent care visits related to hypoglycemia, hyperglycemia, diabetic ketoacidosis (DKA), seizures, or other incidents possibly caused by a malfunctioning G6 or G7 device. - Diabetes Management Records:
Include endocrinology reports that detail your A1c levels and overall diabetes treatment plan. - Data from Devices:
Save downloaded data from your G6 or G7 devices, such as glucose trends, daily summaries, event logs, and alert histories. - Device Details:
Record serial numbers, lot numbers, and expiration dates for sensors and transmitters. Take photographs of the packaging or any adhesive failures for additional evidence.
Who Is Eligible for a Dexcom Recall Lawsuit?
You may qualify for a Dexcom Lawsuit if you:
- Experienced serious health complications due to inaccurate or failed readings by a defective device.
- Required emergency medical treatment or hospitalization if your device malfunctioned.
- Suffered financial losses, such as medical bills or missed work, due to a malfunction by a defective device
- Were not properly warned about known risks of the device
Compensation in a Dexcom Recall Product Lawsuit
If you are eligible for a lawsuit, you to recover damages for:
- Medical expenses (emergency treatment, hospitalization, long-term care)
- Lost wages or reduced earning capacity
- Pain and suffering caused by the defective Dexcom device
- Emotional distress from living with a dangerous medical failure
- Wrongful death damages for families who lost a loved one‘
Frequently Asked Questions
What should I do if I have been affected by the Dexcom Device Recall and am seeking a Nashville Dexcom Recall Lawsuit Lawyer?
If you reside in Nashville and have experienced issues due to a defective Dexcom device that has been subject to a recall, it’s crucial to consult with a qualified Nashville Dexcom Recall Lawsuit Lawyer as soon as possible. A local attorney specializing in Dexcom Device Recall Lawsuits will be familiar with both state and federal regulations regarding medical device recalls, including the FDA recall process.
How do I know if my Dexcom device is part of the current Dexcom Device Recall or subject to a recent Dexcom Device Recall Update?
To determine if your Dexcom device is included in the most recent Dexcom Device Recall or affected by a new Dexcom Device Recall Update, you should check the official recall notices issued by either Dexcom or the U.S. Food and Drug Administration (FDA). These updates provide detailed information about model numbers, lot numbers, and specific batches of recalled Dexcom devices.
If you discover that your device is among those listed as a defective device or recalled Dexcom device, it is important to stop using it immediately and follow the instructions provided in the recall update. Additionally, consider contacting a Dexcom Recall Lawsuit Lawyer for advice about your legal options.
What legal actions can I pursue if I have suffered harm from a defective or malfunctioning Dexcom device included in the recall?
If you have been injured or suffered damages due to a defective Dexcom device—whether through device malfunction or other failures—and that product has been included in the recent Dexcom Device Recall, you may be eligible for compensation through a Dexcom Recall Lawsuit.
An experienced lawyer can help you file a claim against the manufacturer for issues related to defective devices and guide you through the legal process involved in seeking justice. This may include organizing evidence of harm caused by the recalled device, navigating FDA recall procedures, and negotiating settlements on your behalf.
How does the FDA recall process work when addressing issues with defective medical devices like those made by Dexcom?
The FDA recall process is designed to protect consumers from potentially harmful products such as defective medical devices produced by companies like Dexcom. When reports of serious malfunctions or adverse events arise—such as those involving defective or malfunctioning Dexcom devices—the FDA may initiate an investigation that could lead to an official recall announcement.
This process involves notifying healthcare providers and consumers about risks associated with using recalled products (the “Dexcom Device Recall”), outlining steps for returning the product or obtaining replacements, and monitoring corrective actions taken by manufacturers. Keeping up with each new Dexcom Device Recall Update is essential for patients using these devices.
Is there a Dexcom G7 class action lawsuit I can join?
There are two types of class action lawsuits you may be able to join: a consumer class action lawsuit that is suing for refunds of the purchase price of your equipment or subscriptions, or an investor class action that seeks financial damages from securities losses.
How long do I have to file a Dexcom lawsuit?
Each state has a different time limit, and it can be as little as one year from the time you were injured. Make sure you speak to a lawyer to get the exact time limit for your case.
Contact Nashville Dexcom Recall Lawsuit Lawyer Timothy L. Miles Today for a Free Case Evaluation if You Were Injurred by a Defective Dexcom Device
If you or a loved one used a defective Dexcom device and suffered harm when your Dexcom device malfunctioned, contact Nashville Dexcom Recall Lawsuit Lawyer Timothy L. Miles for a free case evaluation today as you may be eligible for a Dexcom Device Recall Lawsuit and potentially be entitled to substantial compensation in a Dexcom Recall Lawsuit. (855) 846–6529 or [email protected].
Timothy L. Miles, Esq.
Law Offices of Timothy L. Miles
Tapestry at Brentwood Town Center
300 Centerview Dr. #247
Mailbox #1091
Brentwood,TN 37027
Phone: (855) Tim-MLaw (855-846-6529)
Email: [email protected]
Website: www.classactionlawyertn.com