GN ReSound 21900500Recalls & reported problems
Gn Hearing A/S · PKG,C-3,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
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05708296217113), received between Mar 2, 2023 and Jul 6, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (3 reports).
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 Device3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 6, 2023Overheating of Device; Overheating of Device
DATE OF INCIDENT IS ESTIMATED DATE (B)(6) 2023. IT HAS BEEN REPORTED THAT- A PATIENT SAID THAT THE CHARGER STARTED SMOKING AND MELTED. NO FURTHER INFORMATION IS AVAILABLE. THIS IS A FINAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17265374 ↗MalfunctionJun 2, 2023Overheating of Device; Overheating of Device
IT WAS REPORTED: PROGRAMMING PROBLEMS. DAMAGED/DEFECTIVE. PATIENT STATES THAT CHARGER WILL NOT CHARGE AND STARTS TO GET HOT AFTER BEING PLUGGED IN FOR SEVERAL MINUTES. 29JUN2023: DATE OF EVENT IS BEST ESTIMATE ((B)(6) 2023) IMAGES OBTAINED OF THE DEVICE SHOWED A MELTED CHARGER PORT. NO FURTHER FOLLOW UP INFORMATION EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17049061 ↗MalfunctionMar 2, 2023Overheating of Device; Overheating of Device
ON (B)(6) 2023, PATIENT NOTICED HEARING AIDS (HA) WERE NOT 100% CHARGING AND WENT TO THEIR HEARING CARE PROVIDER (HCP). HCP NOTICED THAT THE CHARGER HAD MELTED BY THE CONTACT. ORIGINAL EQUIPMENT WAS USED. THERE WERE NO REPORTS OF PATIENT HARM OR INJURY, AND NO MEDICAL INTERVENTION WAS REQUIRED. NO FURTHER INFORMATION IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16465763 ↗
Other Hearing aid, air conduction with wireless technology devices
- GN ReSound 20472100Gn Hearing A/S · Hearing aid, air conduction with wireless technology55 reports
- GN ReSound 21625000Gn Hearing A/S · Hearing aid, air conduction with wireless technology20 reports
- Phonak Brand 050-0889-P5Sonova AG · Hearing Aid, Air Conduction With Wireless Technology8 reports
- GN Hearing 21655200Gn Hearing A/S · Hearing aid, air conduction with wireless technology8 reports
- Beltone 20623200Gn Hearing A/S · Hearing aid, air conduction with wireless technology7 reports
- Beltone 21625700Gn Hearing A/S · Hearing aid, air conduction with wireless technology7 reports
- GN Hearing 20863700Gn Hearing A/S · Hearing aid, air conduction with wireless technology5 reports
- Phonak Audéo I90-Sphere (graphite gray)Sonova AG · Hearing Aid, Air-Conduction With Wireless Technology, Prescription5 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page