GN ReSound 22366472Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296253098), received between Aug 4, 2023 and Aug 4, 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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 4, 2023Overheating of Device; Overheating of Device

  ESTIMATED DATE OF INCIDENT (B)(6) 2023 IT WAS INITIALLY REPORTED THAT THE CHARGER PORT CAUGHT ON FIRE WHERE THE CORD GOES IN HAS MELTED. IT WAS CONFIRMED THAT THERE WAS NO EVIDENCE OR NOTICING OF ACTUAL FLAME IN THIS INCIDENT. THE CHARGER WAS DISCOVERED BY THE PATIENT'S GRANDCHILDREN WHO NOTICED AN "ELECTRICAL BURNING SMELL" WHEN THEY ENTERED THE PATIENT'S HOME. THE CHARGER WAS FOUND TO BE PLUGGED IN AN HAD MELTED. THE PATIENT WAS SLEEPING DURING THE INCIDENT WHILE THE HEARING AIDS WERE IN THE CHARGER. NO ACTUAL FLAMES WERE REPORTED. NO HARM TO THE USER OR PROPERTY HAS BEEN REPORTED. NO DEVICE HAS BEEN SENT. FURTHER FOLLOW UP IS NOT EXPECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17457355 ↗