GN Hearing 21126200Recalls & reported problems
Gn Hearing A/S · CHARGER,LXR,GENERIC,BT INSERT · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296169757), received between Feb 3, 2023 and Feb 3, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (1 report).
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
Device problems
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 3, 2023Overheating of Device; Overheating of Device
ON AN UNKNOWN DATE (BEST ESTIMATE (B)(6) 2023) CHARGER WERE SENT IN WITH COMMENTS SAYING 'CHARGER DEAD'. UPON VIEWING THE PHYSICAL CHARGER IT APPEARS TO BE BADLY DAMAGED AT THE USB PORT AND ON THE USB CABLE. NO HARM TO USER OR DAMAGE TO PROPERTY. THE PATIENT RECEIVED A REPLACEMENT CHARGER AND IS HAPPY WITH IT. NO FURTHER FOLLOW UP INFORMATION EXPECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16290111 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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