Widex MRR2DRecalls & reported problems
Widex A/S · WIDEX MOMENT MRR2D (Golden brown ) 440, RC coil, mRIC R D · 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 05706069884609), received between Mar 19, 2024 and Mar 19, 2024 — classified as 1 injury.
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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IN THIS EVENT, PATIENT INGESTED HER RIGHT HEARING AID, WENT TO HER HCP AND WAS PROVIDED WITH MEDICATION TO AID IN THE "PASSING" OF DEVICE; PATIENT WAS UNABLE TO PASS IT ON HER OWN AND REQUIRED SURGERY TO REMOVE. PATIENT HAD SUCCESSFUL SURGERY TO REMOVE THE INGESTED BATTERY. PATIENT HAD ACCIDENTALLY SWALLOWED THE HEARING AID THINKING THEY WERE PILLS PRIOR TO FALLING ASLEEP. THERE IS A WARNING STATEMENT INCLUDED IN THE DEVICE USER GUIDE IN CASE OF BATTERY BEING SWALLOWED.
Patient problems: Foreign Body In Patient
MAUDE report 18929690 ↗
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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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