Phonak Brand 050-0875-P6Recalls & reported problems
Sonova AG · Phonak Audéo L50-R (silver gray) · Class 2
All models of Phonak Brand (25)
Data updated Oct 18, 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 07613389477702), received between Jun 5, 2024 and Jun 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
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.
MalfunctionJun 5, 2024Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
IT WAS REPORTED THAT UPON REMOVAL OF THE RECEIVER ASSEMBLY FROM THE EAR, THE RECEIVER STUCK IN THE PATIENT'S EAR. THE HCP WAS ABLE TO SUCCESSFULLY REMOVE THE PIECE FROM THE PATIENT'S EAR. THE PATIENT DIDN'T REQUIRE MEDICAL ATTENTION, NOR PRESCRIPTION MEDICATION. THE PATIENT IS DOING WELL AFTER THE REMOVAL. REPORTEDLY, THE RECEIVER BROKE AT THE WIRE CABLE CONNECTION TO THE RECEIVER. THE MANUFACTURER REQUESTED THE DEVICE TO BE SENT BACK FOR ANALYSIS. THIS IS AN INITIAL REPORT. THE SUPPLEMENTAL REPORTS WILL BE SUBMITTED UPON AVAILABILITY OF NEW INFORMATION.
Patient problems: Foreign Body In Patient
MAUDE report 19468580 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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