GN ReSound 19706902Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05704819290175), received between Dec 3, 2020 and Dec 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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.

• MalfunctionDec 3, 2020Device-Device Incompatibility; Device-Device Incompatibility

  AS REPORTED BY LOCAL CUSTOMER SERVICE: LOUD DISTORTION WHEN STREAMING PHONE CALLS; PHONE CALLS OFTEN SOMETIMES SWITCH BETWEEN EARS. IPHONE 12, IOS 14.2. PATIENT REPORTS THAT, EVERY 3RD OR 4TH PHONE CALL, HE HEARS A LOUD DISTORTION. IT WAS LOUD ENOUGH THAT I COULD HEAR IT OVER THE PHONE. PATIENT ALSO REPORTS THAT CALLS OCCASIONALLY DROP FROM ONE EAR. THIS PROBLEM DID NOT OCCUR W/ PATIENT'S PREVIOUS IPHONE. PAIRED DEMO AIDS TO THE IPH 12, SAME THING OCCURRED. DISCUSSED THAT IPH 12 IS NOT ON OUR COMPATIBILITY LIST, IS STILL BEING TESTED. CUSTOMER UNDERSTOOD. GAVE CUSTOMER APPLE ACCESSIBILITY PHONE#. PATIENT WOULD STILL LIKE TO HAVE HAS SENT IN, CUSTOMER WILL SEND ATTN: QE. QUESTIONNAIRE: WAS THE SOUND PAINFUL AND/OR DID IT CAUSE HARM TO THE PATIENT OR OTHER PERSON? NO. HAS THE PATIENT BEEN IN CONTACT WITH A PROFESSIONAL? NO. PLEASE CHOOSE THE DURATION OF THE SOUND? LONGER THAN 10 SECONDS. WHAT TYPE OF RECEIVER? HIGH POWER.

  Patient problems: Partial Hearing Loss; Skin Irritation

  MAUDE report 10940099 ↗