---
title: "Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexc... — FDA record Z-0318-2026 | Is It on Recall"
description: "A software defect in version v1.15.0 of the G6 Android app can cause the app to terminate unexpectedly, which may result in the user not receiving estimated glu"
url: https://isitonrecall.com/recall/fda-device-z-0318-2026-brand-name-dexcom-g6-continuous-glucose-monitoring-system-product-name-dexcom-g6-and-g6-pro-android/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and G6 Pro Android US CGM App Mode... — FDA record Z-0318-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 28, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and G6 Pro Android US CGM App Model/Catalog Number: SW11678 Software Version: version 1.15.0 Product Description: Dexcom G6 and G6 Pro Android US CGM App SW11678 version 1.15.0 Component: Dexcom G6 Continuous Glucose Monitoring System
- **Reason**: A software defect in version v1.15.0 of the G6 Android app can cause the app to terminate unexpectedly, which may result in the user not receiving estimated glucose values, alarms, alerts or notifications. This could result in the missed detection of a hyperglycemic or hypoglycemic event, protentional resulting in severe hyperglycemia, diabetic ketoacidosis (DKA), or hyperosmolar hyperglycemic state (HHS).
- **Classification**: Class I
- **Recalling firm**: Dexcom, Inc.
- **Quantity**: 333
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0318-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0318-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: UDI: SW11678 - 00386270000811 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

This product was distributed throughout the US. G6 Android US v1.15.0 SW11678 G6 and G6 Pro Android app release has been halted

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Nov 5, 2025
- **Recall initiation date**: Aug 28, 2025
- **Center classification date**: Oct 30, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0318-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Dexcom, Inc. records](https://isitonrecall.com/brand/dexcom-inc/)