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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 ↗

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Sources and updates

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