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Beltone RLY2ITC-DW-MPRecalls & reported problems

Gn Hearing A/S · HI,RLY2ITC-DW-MP · Class 2

All models of Beltone (17)

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 05708296208043), received between Apr 19, 2023 and Apr 19, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Leak/Splash” (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

Device problems

  • Leak/Splash1

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.

  • MalfunctionApr 19, 2023Leak/Splash; Leak/Splash

    18-APR-2023: IT WAS REPORTED: "UNSURE IF THE BATTERY ACID HAS CAUSED ANY INTERNAL CIRCUIT DAMAGE". USER DIDN'T PUT AID ON AS NOTICED SOMETHING WAS LEAKING. NO HARM TO USER WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16766918 ↗

Other Hearing aid, air conduction with wireless technology devices

All Hearing aid, air conduction with wireless technology devices →

Sources and updates

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