Phonak Brand 063-0511-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613389452044), received between Jul 20, 2023 and Jul 20, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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.

Most reported problems

Recent adverse event reports

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

• InjuryJul 20, 2023Use of Device Problem; Use of Device Problem

  HEARING AID DISPENSER HAS REPORTED THAT A PATIENT HAS INGESTED A HEARING AID WITH A ZINC-AIR BATTERY INSIDE. IT IS UNKNOWN IF THE RIGHT OR THE LEFT HEARING AID HAS BEEN INGESTED. FOLLOW UP IS ONGOING TO CONFIRM THE PATIENT OUTCOME AND OBTAIN FURTHER INFORMATION ABOUT THE EVENT. SUPPLEMENTARY REPORT WILL BE FILED UPON AVAILABILITY OF FURTHER INFORMATION.

  Patient problems: Foreign Body In Patient

  MAUDE report 17363911 ↗