Glucose monitoring receivers recalled
Certain receivers from Dexcom were recalled because their speakers may fail to make an alert sound.
The FDA reported a class I recall of certain G6, G7, ONE, and ONE+ glucose monitoring receivers by Dexcom, Inc. because a problem with the speaker may cause it to fail to make an alert sound when blood sugar is dangerously low or high. The use of affected product may cause serious adverse health consequences or death. There have been at least 56 reported injuries and no reports of death.
The FDA notification recommends that all users of glucose monitoring receivers test the speakers every time the device is charged, whether or not it is affected by the recall.