PHONAK 050-0439-P5Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613275639900), received between Sep 21, 2026 and Sep 23, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Battery Problem” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjurySep 23, 2026Overheating of Device; Battery Problem

  Patient problems: Skin Burning Sensation

  MAUDE report 50869313 ↗
• InjurySep 21, 2026Overheating of Device; Battery Problem

  Sonova was notified that a hearing aid became hot while being worn by a user, resulting in a burning sensation to the back of the ear. The user removed the device due to the heat. Following the event, the device would not power on or charge and was reported as non-functional.

  Patient problems: Skin Burning Sensation

  MAUDE report 50840843 ↗