Phonak Brand 050-0773-H0Recalls & reported problems
Sonova AG · Phonak Audéo P90-RL (beige) · Class 2
All models of Phonak Brand (25)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613389301113), received between Dec 4, 2025 and Dec 4, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).
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
- Detachment of Device or Device Component2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 4, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT HAS BEEN BROUGHT TO MANUFACTURER'S ATTENTION THAT THE HCP REPORTED SHE NOTICED THE WAX GUARDS DID NOT GO EASILY INTO THE WHEN SHE WENT TO FIT THEM WITH THE PATIENT. THE PATIENT ENDED UP HAVING TO GO TO URGENT CARE BECAUSE THE WAX GUARD FELL OUT AND GOT STUCK IN HIS EAR.
Patient problems: Foreign Body In Patient
MAUDE report 23721241 ↗InjuryDec 4, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT HAS BEEN BROUGHT TO MANUFACTURER'S ATTENTION THAT THE HCP REPORTED SHE NOTICED THE WAX GUARDS DID NOT GO EASILY INTO THE WHEN SHE WENT TO FIT THEM WITH THE PATIENT. THE PATIENT ENDED UP HAVING TO GO TO URGENT CARE BECAUSE THE WAX GUARD FELL OUT AND GOT STUCK IN HIS EAR.
Patient problems: Foreign Body In Patient
MAUDE report 23714503 ↗
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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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