Skip to content

GN ReSound RE9ITE-DW-HPRecalls & reported problems

Gn Hearing A/S · HI,RE9ITE-DW-HP · Class 2

All models of GN ReSound (106)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296174843), received between Sep 21, 2022 and Sep 21, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Abrasion1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 21, 2022Break; Break

    IT WAS REPORTED THE AID WAS NOT FIXED. CUSTOMER STATING PART OF THE SHELL TOWARDS TOP IS STILL BROKEN. THE HEARING AID WORKS BUT CUTTING INTO PATIENTS EAR. COULD STILL SEE SKIN ON THE AID AS WELL. STATING THE AID WAS NOT CLEANED.

    Patient problems: Abrasion

    MAUDE report 15461454 ↗

Other Hearing aid, air conduction with wireless technology devices

All Hearing aid, air conduction with wireless technology devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page