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Phonak Brand 050-1000-P5Recalls & reported problems

Sonova AG · Phonak Audéo L90-RT (champagne) · Class 2

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 07613389478112), received between Dec 20, 2023 and Dec 20, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Overheating of Device” (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

Nov 2023: 0 reportsDec 2023: 1 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Overheating of Device1

Patient problems

  • Headache1
  • Neuralgia1
  • Vertigo1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 20, 2023Overheating of Device; Overheating of Device

    HCP HAS REPORTED THAT A PATIENT HEARD TONES FROM HER HEARING AID AND EXPERIENCED THE DEVICE GETTING VERY HOT AND BURNING HER BEHIND THE EAR. THE PATIENT HAS IMMEDIATELY REMOVED THE DEVICE AND NOTED IT WAS HOT TO TOUCH, ESPECIALLY AT THE BOTTOM, WHERE THE CHARGING CONTACTS ARE LOCATED. AFTER THE INCIDENT THE PATIENT REPORTED HEADACHE, PAIN ABOVE HER RIGHT EYE, AROUND THE RIGHT TEMPLE AND CHEEK BONE, BACK OF HER HEAD AND RIGHT SIDE OF THE NECK. ENT HAS CONFIRMED THAT THERE WAS NO PHYSICAL BURN BUT SUGGESTED THAT THE INCIDENT HAS TRIGGERED A TRIGEMINAL NEURALGIA. THE PATIENT IS BEING TREATED WITH TYLENOL AND PREDNISONE STEROIDS. AS OF DECEMBER 7, THE PATIENT IS STILL EXPERIENCING FACIAL PAIN, HEADACHES AND PAIN ABOVE HER EYE, HOWEVER, THE HEADACHES HAVE IMPROVED, AND THE NECK PAIN HAS RECEDED. THE PATIENT HAS NO HISTORY OF MIGRAINES, HEADACHES, TEETH ISSUES OR CLENCHING OF TEETH. GENERAL STATE OF TEETH WAS GOOD. THE PATIENT HAS DISCONTINUED THE USE OF RECHARGEABLE HEARING AIDS AND SWITCHED TO WEARING AN OLDER NON-RECHARGEABLE MODEL. PATIENT HAS AN APPOINTMENT WITH NEUROLOGIST SCHEDULED IN JANUARY. THIS IS AN INITIAL REPORT. SUPPLEMENTAL INFORMATION WILL BE PROVIDED UPON AVAILABILITY O

    Patient problems: Headache; Neuralgia; Vertigo

    MAUDE report 18363893 ↗

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Sources and updates

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