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
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
- 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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