Widex MBB3D 220Recalls & reported problems
Widex A/S · WIDEX MOMENT MBB3D 220 (Golden brown) · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05706069923254), received between May 17, 2024 and May 17, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Skin Erosion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 17, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
PATIENT UPDATE: PATIENT HAS NOW FULLY RECOVERED IN THIS EVENT; PATIENT WAS CLEANING THE AFFECTED AREA AND APPLYING CREAM TO AID IN THE HEALING PROCESS. PATIENT HAS PRE-EXISTING ATOPIC SKIN CONDITION, WHICH CAUSED THE HEALING PROCESS TO BE DELAYED. INVESTIGATION CONCLUSION: ROOT CAUSE CANNOT BE CONFIRMED BECAUSE THE BATTERY WAS NOT RETURNED.
Patient problems: Skin Erosion
MAUDE report 19341050 ↗
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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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