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Phonak Brand 075-3017-11Recalls & reported problems

Sonova AG · Phonak Charger Case Go (US plug) · Class 2

All models of Phonak Brand (25)

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 07613389329995), received between Aug 21, 2023 and Aug 21, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Temperature 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Temperature Problem1

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.

  • MalfunctionAug 21, 2023Temperature Problem; Temperature Problem

    PATIENT REPORTED TO HCP THAT SHE LEFT A HEARING AID CHARGING CASE ON A NIGHT STAND WHILE SHE WAS AWAY FROM HOME ON A TRIP. WHEN SHE RETURNED HOME, THE CHARGER "MELTED AND DAMAGED HER BED SHEETS AS THEY WERE TOUCHING THE CORD. THE CHARGER HAS BEEN REQUESTED TO BE RETURNED FOR ANALYSIS. SUPPLEMENTAL REPORTS WILL BE SUBMITTED UPON AVAILABILITY OF FURTHER INFORMATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17588100 ↗

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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