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GN ReSound RT5CIC-MPRecalls & reported problems

Gn Hearing A/S · HI,RT5CIC-MP · Class 1

Data updated Oct 13, 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 05708296246700), received between Feb 24, 2023 and Feb 24, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Battery Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Battery Problem1
  • Burst Container or Vessel1

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 24, 2023Burst Container or Vessel; Battery Problem; Burst Container or Vessel; Battery Problem

    ON 24-FEB-2023: ON AN UNKNOWN DATE ((B)(6) 2023 BEST ESTIMATE), IT WAS REPORTED 'BATTERY EXPLODES INSIDE OF HEARING AID'. THE PATIENT WAS CHANGING THE BATTERY WHEN HE NOTICED A POP. HE NEVER HAD THE DEVICE IN HIS EAR, SO THERE WAS NO INJURY. THE BATTERY WAS IN HIS HAND AT THE TIME. ON 23-MAR-2023: 3 ATTEMPTS WERE MADE TO RECEIVE FOLLOW UP INFORMATION. NO FURTHER FOLLOW UP INFORMATION IS EXPECTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16435192 ↗

Other Hearing aid, air conduction devices

All Hearing aid, air conduction devices →

Sources and updates

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