DEXCOM DEVICE RECALL LAWSUIT: A COMPREHENSIVE CONSUMER GUIDE ON EVERYTHING YOU NEED TO KNOW [2026]

TAKE ACTION TODAY:  (855) 846-6529

If you or a loved one used a defective Dexcom device suffered harm when your device malfunctioned, you may be eligible for a Dexcom Recall Lawsuit and potentially be entitled to substantial compensation.  Call Dexcom Recall Lawsuit Lawyer Timothy L. Miles today for a free case evaluation. (855) 846–6529 or [email protected].

SUBMIT YOUR INFORMATION

Key Takeaways

  • The Dexcom Device may pose risks such as false readings, sensor failures, and connectivity issues that endanger patient safety.
  • Class I Recalls (June & Sept 2025—for G6/G7 receivers due to speaker malfunctions that could fail to warn of dangerous glucose levels.
  • Lawsuit Allegations: Plaintiffs allege Dexcom was aware of accuracy issues, failed to warn users, and that the devices failed before the promised 10-day lifespan. Lawsuits, such as those filed in California, seek damages for medical expenses, pain and suffering, and wrongful death.
  • Affected Devices: These include the Dexcom G7, G6, ONE, and ONE+ continuous glucose monitoring systems and their associated apps.
  • Consumers who experienced severe, inaccurate readings or missed alerts may be eligible to participate in the ongoing litigation.
  • Affected users may have legal rights under product liability, negligence, or failure-to-warn claims.
  • Compensation may cover medical bills, lost wages, pain and suffering, and wrongful death damages.
  • If you or a loved one suffered harm from a Dexcom device recall, contact Timothy L. Miles today for a free case evaluation.

Dexcom Device Recall: Check Your Status [2026]

Individuals may confirm if they are using a defective Dexcom device by checking their serial number at Dexcom's official verification portal.

If your device is recalled, contact Dexcom immediately at (844) 478-1600 to request a no-charge replacement.

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 Lawsuitss

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.

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As a direct result of these violations of law,  numerous individuals suffered a device malfunctionwhich resulted in serious injuries and death.

TIMOTHY L. MILES | FREE CASE EVALUATION

TAKE ACTION: CALL TODAY

"It will be the only call you need to make."


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.
 
Class 1 Recall

A Class 1 recall is the most severe type of recall, issued when there is a reasonable probability that using or exposed to a product will cause serious adverse health consequences or death.

Highest Risk: Involves high-risk products, such as undeclared allergens, contamination, or malfunctioning, dangerous devices.
Action Required: Immediate, voluntary, or mandated removal of the product from the consumer level (market) to prevent serious harm.
Scope: Examples include tainted food, mislabeled drugs, and medical devices that could fail and cause injury or death.

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.

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.


If you have questions or are unsure whether youi are eligible for a lawsuit against Dexcom, contact Dexcom Recall Lawsuit Lawyer Timothy L. Miles today foir a free case evaluation and who can answer any questions you may have including whether you qualify for a Lawsuit and could possibly be entitled to substantial compensaation. (855) 846–6529 or [email protected].

Should i Report a Dexcom device malfunctioned?

Yes, the FDA encourages individuals who have experienced problems related to Dexcom to report them through the MedWatch Voluntary Reporting Form or by calling 1-800-332-1088.

Be sure to provide comprehensive details about any defective Dexcom device or other Dexcom device malfunctions you have experienced.

The FDA also advises safely disposing of unused Dexcom at authorized drug take-back locations. If no centers are nearby, follow official FDA instructions for safe disposal.

Compensation in a Dexcom Recall Lawsuit

If you are eligible for a lawsuit, you to recover damages for:

For more information on the type of damages you may be entitled to, contact Dexcom Recall Lawsuit Lawyer Timothy L. Miles today foir a free case evaluation 855) 846–6529 or [email protected].

Contact 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 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.  (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

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Frequently Asked Questions

1.   What Should I Do if I Suffered Injuriesd as a Result of a  Dexcom Device?

  1. Seek medical attention immediately if your health is at risk.
  2. Document everything, including if your device malfunctioned including medical records, and financial costs.
  3. Check recall notices from the FDA or Dexcom to see if your device batch was affected.
  4. Contact Timothy L. Miles to discuss whether you qualify to file a Dexcom lawsuit.

(855) 846–6529 or [email protected].

 

2.   What Type of Damages am I Entitled to if Injured by a Defective Dexcom Device?

Compensation may cover medical bills, lost wages, pain and suffering, and wrongful death damages.

 

3.   What Are the Allegations Against Decxom?

Negliogence, defective design, failure to warn and breach of warrantry have been alleged by those who have filed a Dexcom Lawsuit.

 

4.   What Health Complications and Risks Are Associated with a Defective Dexcom Device?

  • Inaccurate glucose readings

  • Device malfunctions

  • Battery and connectivity issues

  • Severe skin reactions

 

5.  How Do I File a Dexcom Device Recall Lawsuit?

If you are considering filing a lawsuit, your first step is to call Timothy L. Miles for a free case evaluation to see if you qualify for a Dexcom Lawsuit and are potentially entitleed to significant compensation. (855) 846–6529 or [email protected].

SUBMIT YOUR INFORMATION

TIMOTHY L. MILES | FREE CASE EVALUATION

TAKE ACTION: CALL TODAY

"It will be the only call you need to make."