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Widex MOMENT MBR3D 440Recalls & reported problems

Widex A/S · WIDEX MOMENT MBR3D 440 (Titanium Grey) · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05706069870510), received between Mar 22, 2024 and Sep 5, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Material Deformation1
  • Material Integrity Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 5, 2025Material Deformation; Material Deformation

    RESULTS OF TECHNICAL INVESTIGATION: THE BATTERY WAS NOT RETURNED, SO ITS ROLE IN THE INCIDENT CANNOT BE CONFIRMED. EVIDENCE SUGGESTS THE THERMAL EVENT ORIGINATED NEAR THE BOTTOM OF THE DEVICE, SPECIFICALLY IN THE POWER SUPPLY MODULE (PSM) AREA. IT IS IMPORTANT TO NOTE THAT THE PSM WAS NOT RETURNED FOR FURTHER EVALUATION. THE RISK OF A BATTERY CELL SHORTING LEADING TO THE MELTING OF THE HEARING AID HOUSING APPEARS TO BE LOW. A CONCLUSIVE DETERMINATION REGARDING A POTENTIAL DEVICE MALFUNCTION CANNOT BE MADE WITHOUT THE RETURN OF ALL RELEVANT ITEMS AND COMPONENTS. THERE ARE POSSIBLY TWO EXPLANATIONS IN THIS CASE; THE OVERHEATING WAS CAUSED BY EITHER AN EXTERNAL HEAT SOURCE OR FROM A THERMAL RUNAWAY EVENT RESULTING IN THE RAPID RELEASE OF HEAT THAT CHARRED AND DEFORMED NEARBY PLASTIC COMPONENTS. THE PRESENCE OF BURN MARKS ON THE CHARGER SUPPORTS EXTERNAL HEATING. WE WERE INFORMED BY THE USER THAT THE DEVICE WAS PLACED ON A MICROWAVE. THE CHARGER IS STILL FUNCTIONAL AFTER THIS EVENT. ADDITIONALLY, NO FURTHER INFORMATION REGARDING THE BURNED FINGER HAS BEEN RECEIVED FROM THE USER, AND THERE HAVE BEEN NO REPORTS OF MEDICAL INTERVENTION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22976314 ↗
  • MalfunctionMar 22, 2024Material Integrity Problem; Material Integrity Problem

    IN THIS EVENT, THE PATIENT'S HEARING AIDS AND CHARGER MELTED WHILE CHARGING. INVESTIGATION RESULTS: CHARGER WITH ACCESSORIES AND HEARING AIDS WERE RETURNED FOR INVESTIGATION. NO SIGN OF MELTED OR BURNT PART ON THE EXTERNAL AREA OF THE CHARGER. POWER ADAPTER AND CABLE CONNECTOR HAVE NO VISUAL DEFECT AND NO SIGN OF BURNT/ MELTED PART. POWER ADAPTER HAS GOOD VOLTAGE OUTPUT BUT IS NOT A WSA PRODUCT. SAFETY INFORMATION IN USER GUIDE, INSTRUCTS USER TO ONLY USE A WIDEX POWER ADAPTER AND CABLE WITH CHARGER. CANNOT DIAGNOSE HEARING AIDS AS BOTH ARE ALREADY STUCK INSIDE THE CHARGING WELLS, WITH SOME PARTS MELTED. ONE OF THE HEARING AID'S BATTERY ALREADY EXPLODED. INTERNAL COMPONENTS OF THE CHARGER HAS SIGNS OF MELTING/BURNING. 2ND LEVEL INVESTIGATION TO BE PERFORMED TO DETERMINE WHAT WENT WRONG IN THE CHARGER'S INTERNAL COMPONENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18961878 ↗

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Sources and updates

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