Phonak Brand 050-0818-P6Recalls & reported problems
Sonova AG · Naida Naída P90-UP (silver gray) · 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 07613389360110), received between May 21, 2022 and May 21, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Unexpected Therapeutic Results” (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.
Most reported problems
Device problems
- Unexpected Therapeutic Results2
Patient problems
- Acoustic Trauma2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 21, 2022Unexpected Therapeutic Results; Unexpected Therapeutic Results
ON 19.05.2022 PATIENT HAS BEEN FITTED WITH NAIDA P90-UP HEARING AIDS ON THE 19.04.2022. LATER IN THE EVENING THE PATIENT REPORTED SUDDEN LOSS OF HEARING AND A CONSTANT RINGING IN THE EARS AFTER MAKING A PHONE CALL. HEARING AID PROVIDER HAS SEEN THE PATIENT ON 20.04.2022 AND REFERRED TO ENT WITH A REPORT OF TINNITUS AND VERTIGO. ON 21.04.2022 AFTER AN ENT VISIT THE PATIENT HAS INFORMED THE PROVIDER THAT HE WAS DIAGNOSED WITH ACOUSTIC TRAUMA. SUPPORTING MEDICAL REPORT PROVIDED. ON 25.04.2022 SUGGESTS A POSSIBLE ACOUSTIC TRAUMA DUE TO THE PATIENT HAVING A NARROW DYNAMIC RANGE AND RECEIVING TOO MUCH SOUND OUTPUT. PATIENT HAS BEEN PRESCRIBED STEROIDS AND RETURNED TO USING THE HEARING AIDS HE HAD BEFORE THE FITTING OF NEW NAIDA P90-UP.
Patient problems: Acoustic Trauma
MAUDE report 14464583 ↗InjuryMay 21, 2022Unexpected Therapeutic Results; Unexpected Therapeutic Results
ON 19.05.2022 PATIENT HAS BEEN FITTED WITH NAIDA P90-UP HEARING AIDS ON THE 19.04.2022. LATER IN THE EVENING THE PATIENT REPORTED SUDDEN LOSS OF HEARING AND A CONSTANT RINGING IN THE EARS AFTER MAKING A PHONE CALL. HEARING AID PROVIDER HAS SEEN THE PATIENT ON 20.04.2022 AND REFERRED TO ENT WITH A REPORT OF TINNITUS AND VERTIGO. ON 21.04.2022 AFTER AN ENT VISIT THE PATIENT HAS INFORMED THE PROVIDER THAT HE WAS DIAGNOSED WITH ACOUSTIC TRAUMA. SUPPORTING MEDICAL REPORT PROVIDED. ON 25.04.2022 SUGGESTS A POSSIBLE ACOUSTIC TRAUMA DUE TO THE PATIENT HAVING A NARROW DYNAMIC RANGE AND RECEIVING TOO MUCH SOUND OUTPUT. PATIENT HAS BEEN PRESCRIBED STEROIDS AND RETURNED TO USING THE HEARING AIDS HE HAD BEFORE THE FITTING OF NEW NAIDA P90-UP.
Patient problems: Acoustic Trauma
MAUDE report 14464531 ↗
Other Hearing aid, air conduction with wireless technology devices
- GN ReSound 20472100Gn Hearing A/S · Hearing aid, air conduction with wireless technology55 reports
- GN ReSound 21625000Gn Hearing A/S · Hearing aid, air conduction with wireless technology20 reports
- GN Hearing 21655200Gn Hearing A/S · Hearing aid, air conduction with wireless technology8 reports
- Phonak Brand 050-0889-P5Sonova AG · Hearing Aid, Air Conduction With Wireless Technology8 reports
- Beltone 20623200Gn Hearing A/S · Hearing aid, air conduction with wireless technology7 reports
- Beltone 21625700Gn Hearing A/S · Hearing aid, air conduction with wireless technology7 reports
- Phonak Audéo I90-Sphere (graphite gray)Sonova AG · Hearing Aid, Air-Conduction With Wireless Technology, Prescription5 reports
- GN Hearing 20863700Gn Hearing A/S · Hearing aid, air conduction with wireless technology5 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.
How reports and recalls are matched · Editorial policy · Report an error on this page