Beltone 21625700Recalls & reported problems
Gn Hearing A/S · PKG,CHGR STD,C-2,BT,CFF1,US · Class 2
All models of Beltone (17)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 05708296200139), received between Dec 29, 2022 and Aug 21, 2023 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (7 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
Device problems
- Overheating of Device7
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 21, 2023Overheating of Device; Overheating of Device
ESTIMATED DATE OF INCIDENT (B)(6) 2023. IT WAS REPORTED THAT THE CHARGER ALLEGEDLY FRIED/BURNED AT THE CHARGING PORT. THERE WAS NO HARM TO THE USER, AND NO REPORTED PROPERTY DAMAGE. NO FURTHER FOLLOW UP IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17583941 ↗MalfunctionAug 1, 2023Overheating of Device; Overheating of Device
ESTIMATED DATE OF INCIDENT (B)(6) 2023: IT WAS REPORTED THAT THE CHARGER EXPLODED AND MELTED AT CHARGER CONNECTION WHILE PLUGGED INTO A CAMPER OUTLET. ORIGINAL ACCESSORIES WERE USED. NO HARM TO THE USER OR PROPERTY HAS BEEN REPORTED. NO FURTHER FOLLOW UP IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17434535 ↗MalfunctionJul 17, 2023Overheating of Device; Overheating of Device
ESTIMATED DATE (B)(6) 2023. (B)(6) 2023, IT HAS BEEN REPORTED- CHARGER CAUGHT ON FIRE. FURTHER INFORMATION IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17331884 ↗MalfunctionJul 13, 2023Overheating of Device; Overheating of Device
ESTIMATED DATE OF INCIDENT 01-APR-2023. IT IS REPORTED THAT THE CHARGER MELTED AT USB PORT. THERE WAS NO HARM TO THE USER. NO PROPERTY DAMAGE REPORTED. AWARENESS DATE: 14JUN2023. FURTHER FOLLOW UP IS EXPECTED. 10AUG2023 NO FURTHER FOLLOW UP RECEIVED. NO FURTHER FOLLOW UP IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17314724 ↗MalfunctionApr 19, 2023Overheating of Device; Overheating of Device
IT IS REPORTED THAT: ESTIMATED DATE OF INCIDENT (B)(6) 2023. FOR A HEARING AID CHARGER CAUGHT ON FIRE WHERE CORD PLUGS INTO CHARGER. NO HARM DONE TO THE PATIENT OR TO THEIR HOME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16767068 ↗MalfunctionMar 10, 2023Overheating of Device; Overheating of Device
IN (B)(6) 2023 (BEST ESTIMATE), PATIENT REPORTED THAT SHE WOKE UP TO HER CHARGER SMOKING. CHARGER WAS PLUGGED AND WAS SMOKING. ORIGINAL EQUIPMENT WAS USED. THERE WERE NO REPORTS OF PATIENT HARM OR INJURY, AND NO MEDICAL INTERVENTION WAS REQUIRED. NO FURTHER INFORMATION IS EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16520796 ↗MalfunctionDec 29, 2022Overheating of Device; Overheating of Device
ON 01-DEC-2022 IT WAS REPORTED THAT A PATIENT ON AN UNKNOWN DATE PLUGGED IN THE CHARGER AND STARTED SMELLING LIKE IT WAS BURNING. FOLLOW UP INFORMATION RECEIVED ON 21-DEC-22: THE PATIENT HAD THE CHARGE PLUGGED IN TO CHARGE THE AIDS AND STARTED SMELLING A BURNING SMELL, THE CHARGER WAS PLACED ON THE DESK. THE ORIGINAL CHARGER WAS USED, UNSURE IF THE CORD WAS ORIGINAL. THE DEVICE WAS BOUGHT ON (B)(6) 2021 IN (B)(6) US. NO HARM TO THE PATIENT REPORTED AND NO CONTACT WITH AUTHORISED MEDICAL PRACTITIONER. HEARING CARE PROFESSIONAL RECOMMENDED TO EXCHANGE FOR A DIFFERENT CHARGER. THE REPLACEMENT(S) SHIPPED TO CUSTOMER ON (B)(6) 2022. 26-JAN-2023: NO FURTHER INFORMATION RECEIVED, NOR EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16066606 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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