GN Hearing 22421100Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05708296255153), received between May 25, 2023 and May 26, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• MalfunctionMay 26, 2023Overheating of Device; Overheating of Device

  ON AN UNKNOWN DATE ((B)(6) 2023 BEST ESTIMATE) CHARGER WAS PLUGGED INTO BATHROOM WALL OUTLET AND THE BACK CONNECTION MELTED. ORIGINAL EQUIPMENT WAS USED. THERE HAS BEEN NO HARM TO THE PATIENT OR PROPERTY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17009296 ↗
• MalfunctionMay 25, 2023Overheating of Device; Overheating of Device

  IT WAS REPORTED: USER WAS "TRYING TO GET USED TO THE HEARING AIDS" SO DOESN'T WEAR EVERY DAY - IN FACT LEAVES THEM IN CHARGER, PLUGGED INTO A POWER STRIP FOR 3-4 DAYS. SHE NOW REPORTS A "BURNING SMELL AND THE AIDS ARE HOT" AND NO LONGER TURN ON. NO FURTHER INFORMATION REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17001397 ↗