Beltone 21790400Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05708296214457), received between Sep 14, 2022 and May 16, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 16, 2023Overheating of Device; Overheating of Device

  IT WAS REPORTED- ACHIEVE CHARGER MELTED CHARGER WAS BROUGHT ON (B)(6) 2023. NO HARM DONE TO THE PATIENT OR PROPERTY. ORIGINAL EQUIPMENT WAS USED. RECOMMENDATION FROM THE HCP: USE CHARGER AS PER THE INSTRUCTIONS. DO NOT USE ANY OTHER USB CABLES OR PLUGS OTHER THAN WHAT CAME WITH THE CHARGER (MORE OF A REMINDER SINCE THE INCIDENT DID NOT INVOLVE ANY AFTER MARKET PARTS).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16937914 ↗
• MalfunctionOct 6, 2022Overheating of Device; Overheating of Device

  ON AN UNKNOWN DATE ((B)(6) 2022 BEST ESTIMATE) THE CHARGER MELTED WHERE THE CORD PLUGS IN. IT WAS HOT TO THE TOUCH. NO PERSONAL INJURY OR PROPERTY DAMAGE SUSTAINED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15548968 ↗
• MalfunctionSep 14, 2022Overheating of Device; Overheating of Device

  ON 13-SEP-2022: IT WAS REPORTED THAT WHEN HEARING AIDS WERE CHARGING OVERNIGHT INTO THE NEXT MORNING THE CHARGER WAS MELTED. THE INCIDENT HAPPENED ON (B)(6) 2022, AND WAS REPLACED THE SAME DAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15416763 ↗