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Beltone IMG6ITE-DWC-MPRecalls & reported problems

Gn Hearing A/S · HI,IMG6ITE-DWC-MP · Class 2

All models of Beltone (17)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296217564), received between Jun 21, 2023 and Jun 21, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Overheating of Device” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Overheating of Device1

Patient problems

  • Skin Burning Sensation1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 21, 2023Overheating of Device; Overheating of Device

    ON (B)(6) 2023 (BEST ESTIMATE) IT WAS ALLEGED THAT PATIENT'S RIGHT HEARING AID WAS "BURNING HOT" AFTER A NIGHT IN THE CHARGER. PATIENT DROPPED THEM BECAUSE IT WAS SO "SO HOT THAT HE BURNED HIMSELF ON IT". FOLLOW UP INFORMATION RECEIVED : "THERE WAS A LITTLE BIT OF RED ON ONE FINGER, BUT IT WASN'T MUCH. PHOTO IS PROBABLY NO LONGER POSSIBLE AS IT IS GONE NOW. BUT IT WASN'T THAT BAD".

    Patient problems: Skin Burning Sensation

    MAUDE report 17171802 ↗

Other Hearing aid, air conduction with wireless technology devices

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Sources and updates

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