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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Monitoring Devices

Dexcom G6 Android App Recalled for Software Defect Disabling Glucose Alerts

Agency Publication Date: October 30, 2025
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Summary

Dexcom, Inc. is recalling 333 units of its Dexcom G6 and G6 Pro Android app (version 1.15.0) because of a software defect that can cause the application to shut down unexpectedly. If the app stops running, users will not receive glucose readings, alarms, or notifications. This issue was identified during a limited rollout, affecting less than 1% of the intended distribution, and the manufacturer has halted further releases of this version.

Risk

If the application terminates unexpectedly, consumers may miss critical detection of high or low blood sugar levels. This could lead to serious life-threatening conditions, including severe hyperglycemia, diabetic ketoacidosis (DKA), or hyperosmolar hyperglycemic state (HHS).

What You Should Do

  1. This recall affects the Dexcom G6 and G6 Pro Android app (Model SW11678, version 1.15.0) used with the Dexcom G6 Continuous Glucose Monitoring System.
  2. Check the settings or 'About' section within your Dexcom G6 Android app to confirm if you are using software version 1.15.0.
  3. Stop using the product. Return it to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or the manufacturer for further instructions.
  4. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: Dexcom G6 and G6 Pro Android US CGM App
Variants: Software Version 1.15.0
Model / REF:
SW11678
Lot Numbers:
Code
UDI:
00386270000811

Recall pertains specifically to software version v1.15.0; rollout was halted at less than 1% completion.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97607
Status: Active
Manufacturer: Dexcom, Inc.
Manufactured In: United States
Units Affected: 333
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.