GN Hearing 20896300Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05708296156160), received between Oct 11, 2022 and Jan 5, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionJan 5, 2023Overheating of Device; Overheating of Device

  03-JAN-2023: ON AN UNKNOWN DATE (BEST ESTIMATE: (B)(6) 2022) CHARGER BURNT AT CHARGING PORT. THERE WAS NO PATIENT HARM. ORIGINAL ACCESSORIES/EQUIPMENTS WERE USED. NO FURTHER INFORMATION EXPECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16101001 ↗
• MalfunctionOct 11, 2022Overheating of Device; Overheating of Device

  IT WAS REPORTED- CHARGER GOT SO HOT IT MELTED AT THE CHARGING PORT. SHE IS NOT SURE IF THE CABLE AND WALL ADAPTER ARE OURS. SHE WILL SEND IN WITH COMPLAINT CASE # - IT IS OUT OF WARRANTY. THE AUDIOLOGIST DID NOT KNOW IF THE HA INSIDE THE CHARGER. THE EXACT DATE OF INCIDENT IS UNKNOWN. THIS IS A COMBINED (INITIAL AND FINAL) REPORT. NO FURTHER FOLLOW UP IS EXPECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15578409 ↗