GN ReSound 19706501Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05704819289605), received between Sep 14, 2020 and Sep 14, 2020 — classified as 1 malfunction.

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 14, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED BY THE LOCAL HEARING AID DEALER: AIDS BEEP "A COUPLE TIMES AND THEN 'BOOM! THEY GET REAL LOUD" - PAINFUL. PATIENT HAS NOT SEEN PHYSICIAN AND HAS CONTINUED TO WEAR AIDS BUT THEY SUDDENLY GET REALLY LOUD. NO EXPLANATION WITH CURSORY REVIEW OF SETTINGS EXCEPT CR'S VERY HIGH AND ERRATIC, REACHING GAIN CURVE AT SOME FREQUENCIES. HAVE THE SYMPTOM(S) DISAPPEARED COMPLETELY? YES.

  Patient problems: Partial Hearing Loss; Skin Irritation

  MAUDE report 10526989 ↗