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GN ReSound 22345400Recalls & reported problems

Gn Hearing A/S · CHGR CUSTOM,C-4,RS,VA · Class 2

All models of GN ReSound (106)

Data updated Oct 18, 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 05708296251261), received between Jun 20, 2023 and Jun 20, 2023 — 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 18, 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.

  • MalfunctionJun 20, 2023Overheating of Device; Overheating of Device

    22MAY2023 IT WAS REPORTED THAT CHARGER OVERHEATED "MELTED AND BLACK IN SOME AREAS". CLINICIAN WAS UNABLE TO CONFIRM IF PROPER CHARGING CABLE WAS BEING USED. NO INJURIES TO PATIENT OR PROPERTY. THIS IS A COMBINED REPORT. NO FURTHER FOLLOW UP IS EXPECTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17162731 ↗

Other Hearing aid, air conduction with wireless technology devices

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Sources and updates

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