GN ReSound 20686204Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296145362), received between Sep 27, 2022 and Sep 27, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Excessive Heating” (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.

• MalfunctionSep 27, 2022Excessive Heating; Excessive Heating

  MANUFACTURER'S REF: SF (B)(4). IT HAS BEEN REPORTED- HEARING AID HEATED UP IN THE CHARGER SO BADLY THAT IT BURNT THE PATIENT'S FINGER WHEN SHE REMOVED FROM CHARGER ENOUGH TO TURN HER FINGER RED WHERE SHE MADE CONTACT. NO FURTHER INFORMATION AVAILABLE REGARDING PICTURES, TREATMENT, ETC. THIS IS A FINAL REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; Superficial (First Degree) Burn

  MAUDE report 15493452 ↗