GN ReSound RT9ITC-DWC-HPRecalls & reported problems
Gn Hearing A/S · HI,RT9ITC-DWC-HP · Class 2
All models of GN ReSound (106)
Data updated Oct 16, 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 05708296217861), received between Feb 1, 2024 and Feb 1, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 1, 2024Fracture; Fracture
ESTIMATED DATE OF INCIDENT (B)(6) 2023 IT WAS REPORTED THAT THE USER'S IN-THE-EAR HEARING AID HAD CRACKED FOR THE SECOND TIME. DATE OF AWARENESS: 04TH JAN 2024: ON 04JAN2024 THE DEVICE WAS RECEIVED BACK BY MANUFACTURER, AND IT BECAME APPARENT THAT THE BREAK ON THE HEARING AID WAS INSIDE THE EAR CANAL, AND THEREFORE COULD LEAD TO A SERIOUS INJURY, IF THE USER WERE TO CONTINUE WEARING THE DEVICE. NO HARM TO THE USER OR PROPERTY HAS BEEN REPORTED. NO FURTHER FOLLOW UP IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18621574 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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