Phonak Brand 063-0002-01Recalls & reported problems
Sonova AG · Phonak Virto P90-10 NW O · Class 1
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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613389451948), received between Aug 15, 2024 and Aug 15, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Eczema1
- 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.
InjuryAug 15, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
WHEN THE PATIENT REMOVED HIS HEARING AID FROM THE EAR, THE FACEPLATE WAS TAKEN OFF AND A LITTLE FRAGMENT WAS STUCK IN THE EAR. THE PATIENT HAD TO GO TO A HOSPITAL TO HAVE THE PIECE REMOVED. THE PATIENT HAD ECZEMA IN THE TYMPANIC MEMBRANE AND EXTERNAL AUDITORY CANAL. THE PATIENT WAS PRESCRIBED CETRAXAL THAT HE NEEDS TO APPLY FOR 5 DAYS.
Patient problems: Eczema; Foreign Body In Patient
MAUDE report 19990011 ↗
Other Hearing Aid, Air Conduction devices
- Phonak Lyric4 (L)Sonova AG · Hearing Aid, Air-Conduction, Prescription14 reports
- Phonak Lyric4 (S)Sonova AG · Hearing Aid, Air-Conduction, Prescription11 reports
- Phonak Lyric4 (M)Sonova AG · Hearing Aid, Air-Conduction, Prescription7 reports
- GN Hearing 21385500Gn Hearing A/S · Hearing Aid, Air-Conduction, Prescription6 reports
- Phonak Lyric4 (XS)Sonova AG · Hearing Aid, Air-Conduction, Prescription6 reports
- Phonak Lyric4 (XL)Sonova AG · Hearing Aid, Air-Conduction, Prescription6 reports
- Phonak Lyric4 (XXS)Sonova AG · Hearing Aid, Air-Conduction, Prescription6 reports
- PHONAK 078-0060Sonova AG · Hearing aid, air conduction4 reports
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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