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GN Hearing 22232804Recalls & reported problems

Gn Hearing A/S · HI,XC361-DRWC,HBM,DBR · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296237821), received between Dec 7, 2022 and Dec 7, 2022 — classified as 1 malfunction.

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 16, 2026.

Most reported problems

Device problems

  • Overheating of Device1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionDec 7, 2022Overheating of Device; Overheating of Device

    06-DEC-2022: ON UNKNOWN DATE (BEST ESTIMATE (B)(6) 2022) CHARGER CAUGHT FIRE. CHARGER MELTED ON THE SIDE WHERE THE CORD PLUGS INTO THE CHARGER ITSELF. THIS WAS DURING THE CHARGING OF THE HEARING AID. NO HARM REPORTED AND NO VISIT TO THE DOCTOR. RECHARGEABLE BATTERIES WERE USED. THE ORIGINAL ACCESSORIES/EQUIPMENT WAS USED. THE HEARING AIDS WERE REPLACED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15929944 ↗

Other Hearing aid, air conduction with wireless technology devices

All Hearing aid, air conduction with wireless technology devices →

Sources and updates

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