Phonak Brand 050-0807-H0Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613389358513), received between May 17, 2023 and May 17, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 17, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  HCP REPORTED THAT THE PATIENT EXPERIENCED DIZZINESS TWO DAYS AFTER COMMENCING THE USE OF THE PHONAK NAIDA P30-PR HEARING AIDS, AND HAS BEEN HOSPITALIZED DUE TO THE SYMPTOMS. REPORTEDLY,THE HOSPITAL STATED THAT THE CAUSE OF THE ISSUE IS LIKELY TO BE OVER AMPLIFIED SOUND FROM THE HEARING AIDS. THE PATIENT DID NOT RETURN TO USING THE REPORTED HEARING AIDS AND HAS BEEN RE-FIT WITH RIC DEVICES IN (B)(6) 2023. PATIENT HAS HAD NO COMPLAINTS OF DIZZINESS SINCE THE ORIGINAL EPISODE. THIS IS AN INITIAL REPORT. THE INVESTIGATION IS ONGOING. SUPPLEMENTAL REPORTS WILL BE SUBMITTED UPON AVAILABILITY OF FURTHER INFORMATION.

  Patient problems: Dizziness

  MAUDE report 16947752 ↗
• InjuryMay 17, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  HCP REPORTED THAT THE PATIENT EXPERIENCED DIZZINESS TWO DAYS AFTER COMMENCING THE USE OF THE PHONAK NAIDA P30-PR HEARING AIDS, AND HAS BEEN HOSPITALIZED DUE TOTHE SYMPTOMS. REPORTEDLY,THE HOSPITAL STATED THAT THE CAUSE OF THE ISSUEIS LIKELY TO BE OVER AMPLIFIED SOUNDFROM THE HEARING AIDS. THE PATIENT DID NOT RETURN TO USING THE REPORTED HEARING AIDS AND HAS BEEN RE-FIT WITH RIC DEVICES IN (B)(6) 2023. PATIENT HAS HAD NO COMPLAINTS OF DIZZINESS SINCE THE ORIGINAL EPISODE. THIS IS AN INITIAL REPORT. THE INVESTIGATION ISONGOING. SUPPLEMENTAL REPORTS WILL BE SUBMITTED UPON AVAILABILITY OF FURTHER INFORMATION.

  Patient problems: Dizziness

  MAUDE report 16947751 ↗