GN ReSound 21973300Recalls & reported problems
Gn Hearing A/S · PKG,CHG KIT,CO,PREM3,CFF3,US · 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 05708296218868), received between Jul 7, 2023 and Jul 7, 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.
MalfunctionJul 7, 2023Overheating of Device; Overheating of Device
IT HAS BEEN REPORTED THAT ON (B)(6) 2023 (ESTIMATED DATE)- CHARGER WITH USB PORT SN (B)(6) WAS REPORTED BY MEMBER TO BE SMOKING AND CABLE MELTED. MEMBER WAS ABLE TO WEAR HEARING AIDS WITHOUT A PROBLEM. NO FURTHER INFORMATION GIVEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17277717 ↗
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- GN Hearing 20863700Gn Hearing A/S · Hearing aid, air conduction with wireless technology5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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