Unitron 050-6269-P6Recalls & reported problems
Unitron Hearing Division · DX Moxi Jump R T 5 (platinum) · 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 07613389340587), received between Dec 9, 2024 and Dec 9, 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.
InjuryDec 9, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE PATIENT ACCIDENTALLY SWALLOWED ONE HEARING AID WHILE HE WAS ASLEEP. HE WOKE UP WITH A VERY SORE THROAT AND ONE OF HIS HEARING AIDS WAS MISSING. IT WAS REPORTED THAT THE PATIENT USUALLY STORES HIS HEARING AIDS IN A CHARGER AT NIGHT AND THAT THE PATIENT MIGHT HAVE CONFUSED THEM FOR HIS PILLS WHILE DREAMING. THE PATIENT WENT TO THE HOSPITAL AND X-RAY EXAMINATION CONFIRMED THAT THE HEARING AID IS IN PATIENT'S SMALL INTESTINE. AT THE TIME OF THIS REPORT, NO FURTHER HARM OR INJURY WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 20876822 ↗
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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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