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GN ReSound 21810900Recalls & reported problems

Gn Hearing A/S · PKO,CHGR PREM3,C-1,RS,CFF3,US · Class 2

All models of GN ReSound (106)

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 05708296217069), received between Jul 6, 2023 and Jul 6, 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 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.

  • MalfunctionJul 6, 2023Overheating of Device; Overheating of Device

    ESTIMATED DATE OF INCIDENT (B)(6) 2023 IT WAS REPORTED THAT THE CHARGER PORT CAUGHT ON FIRE AND MELTED. NO HARM TO THE USER OR PROPERTY HAS BEEN REPORTED. FURTHER FOLLOW UP IS EXPECTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17265010 ↗

Other Hearing aid, air conduction with wireless technology devices

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Sources and updates

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