> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Dexcom Recalls Dexcom Glucose Monitor Receivers
- URL: https://www.fdaweb.com/dexcom-recalls-dexcom-glucose-monitor-receivers/
- Published: 2025-07-17T12:00:00.000Z
- Updated: 2026-09-14T15:16:54.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5159528

Dexcom is recalling (Class 1) certain Dexcom G6, G7, ONE, and ONE+ glucose monitoring receivers because a speaker problem may prevent an alert from sounding when blood sugar is dangerously low or high. “The use of affected product may cause serious adverse health consequences, including seizures, vomiting, loss of consciousness, and death,” a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/continuous-glucose-monitor-receiver-recall-dexcom-inc-removes-certain-dexcom-g6-g7-one-and-one?utm%5Fmedium=email&utm%5Fsource=govdelivery) says. To date, the company has received 56 injury reports.

The receivers are part of continuous glucose monitoring systems that help people with diabetes track glucose levels in real time, the alert says, adding that they issue alerts when blood sugar is too high or too low.