GN ReSound RT9ITE-DWC-MPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296217915), received between Jan 16, 2024 and Jan 16, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-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 18, 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.

• InjuryJan 16, 2024Patient-Device Incompatibility; Patient-Device Incompatibility

  ESTIMATED DATE OF INCIDENT 04-SEP-2023. IT WAS REPORTED THAT THE USER ON (B)(6)2023 STARTED TO GET IRRITATION IN HER CONCHA BOWL IN (B)(6) 2023. SYMPTOMS INCLUDED REDNESS, PAIN, SORES AND INFLAMMATION ON ONE EAR. USER IS WEARING SAME TYPE OF HEARING AID OF THE OTHER EAR, BUT WITH NO ECZEMA AT THIS TIME. THE USER HAS A HISTORY OF ECZEMA SINCE 2020. THE USER HAS BEEN WEARING THE HEARING AIDS SINCE NOVEMBER OF 2022. THIS ECZEMA FLARE UP BEGAN IN (B)(6) 2023. THE USER SAW HER GENERAL PRACTITIONER WHO REFERRED HER TO HER EAR-NOSE-THROAT-DOCTOR AND THIS PERSON REFERRED HER TO A DERMATOLOGIST. OFFICIAL DIAGNOSIS FROM DERMATOLOGIST IS ECZEMA. USER HAS BEEN TREATED WITH HYDROCORTISONE, ANTIFUNGAL MEDICATION AND STEROID DROPS.

  Patient problems: Eczema

  MAUDE report 18519379 ↗