GN ReSound 20413909Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05708296145188), received between Jun 24, 2020 and Nov 4, 2022 — classified as 2 malfunctions.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 4, 2022Overheating of Device; Overheating of Device

  HEARING AIDS WERE IN CHARGER OVERNIGHT. WHEN PATIENT OPENED CHARGER THE NEXT DAY, THE RECEIVER WAS MELTED INSIDE OF CHARGER (OVERHEATED). THERE WAS NO HARM TO PATIENT. APPROXIMATES THAT THE INCIDENT HAPPENED AROUND THE WEEK OF ON (B)(6) 2022. ORIGINAL GN CHARGER USED. DEVICES WERE REPLACED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15725078 ↗
• MalfunctionJun 24, 2020Patient-Device Incompatibility; Patient-Device Incompatibility

  NO ADDITIONAL INFORMATION REGARDING THE PATIENT AND/OR EVENT HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.

  Patient problems: Hearing Impairment; No Clinical Signs, Symptoms or Conditions

  MAUDE report 10188525 ↗