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GN ReSound 21588900Recalls & reported problems

Gn Hearing A/S · PKG,CHGR PREM2,C-1,RS,CFF1,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 05708296200375), received between Aug 17, 2022 and Aug 17, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1
  • Overheating of Device1
  • Temperature Problem1

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 17, 2022Overheating of Device; Temperature Problem; Insufficient Device Problem Information; Overheating of Device; Temperature Problem; Insufficient Device Problem Information

    ON (B)(6) 2022 IT WAS REPORTED 'CHARGER IS GETTING HOT AND MELTED AT THE CHARGER PORT'. THE CUSTOMER REPORTED 'MY CHARGER SHORTED OUT AND MELTED THE OTHER DAY' THERE IS NO HARM TO THE CUSTOMER REPORTED. FOLLOW UP INFORMATION WILL BE SUBMITTED ONCE COMPLETED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15238707 ↗

Other Hearing aid, air conduction with wireless technology devices

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Sources and updates

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