GN ReSound 21587700Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296200337), received between Oct 14, 2022 and Oct 14, 2022 — 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.

• MalfunctionOct 14, 2022Overheating of Device; Overheating of Device

  REF (B)(4). ON 13SEP2022: IT WAS REPORTED HEARING AID CHARGER AND USB-C CONNECTOR MELTED AND "FUSED" TOGETHER SO THE USB-C CABLE COULD NOT BE REMOVED AND CABLE BROKE. ONLY ORIGINAL EQUIPMENT WAS USED. THE RECHARGABLE HEARING AIDS WITHT HE CHARGER WERE PURCHASED ON (B)(6) 2021. THE DATE OF THE INCIDENT IS NOT AVAILABLE. DEVICE IS OUT OF WARRANTY, THE CLINIC PURCHASED A NEW DEVICE. THE DATE OF THE EVENT IS NOT AVAILBLE. NO PATIENT INVOLVMENT OR HARM TO THE USER REPORTED. ON 09NOV2022: NO NEW INFORMATION RECIEVED. NO FOLLOW UP IS EXPECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15604245 ↗