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GN ReSound 22357500Recalls & reported problems

Gn Hearing A/S · PKG,C-2 GEN,RS,CFF6,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 05708296252756), received between Aug 2, 2023 and Aug 2, 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.

  • MalfunctionAug 2, 2023Overheating of Device; Overheating of Device

    DATE OF INCIDENT (B)(6) 2023. IT WAS REPORTED THAT THE BACK OF THE CHARGER HAD MELTED, AND WAS SMOKING. ORIGINAL ACCESSORIES WERE USED. CHARGER WAS PLUGGED INTO AN END TABLE, WITH CHARGING USB BUILT IN AT THE TIME OF THE INCIDENT. NO HARM TO THE USER OR PROPERTY HAS BEEN REPORTED. THE CHARGER WAS BOUGHT 2-28-23 WITH HEARING AID PURCHASE. NO FURTHER FOLLOW UP IS EXPECTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17441642 ↗

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Sources and updates

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